Clinical research courses are necessary to ensure that there are enough competent, responsible, and efficient clinical research professionals in the clinical research field. In this article, we'll be paying attention to the clinical research courses for Clinical Trial Assistants (CTAs), and Junior or Senior Clinical Research Associates (CRAs).

CTA

CTAs are one of the crucial role players in the clinical research process. They maintain the project's records, files, documentation and store them. They also assist with the review of clinical project records for accuracy and make them complete and ready for audit.

The CTA course offered at CCRPS are for those who are new to the job and want to cover the basics and principles of clinical research.

The program will highlight ICH GCP as the clinical research basis to introduce the new CTAs to drug development and to be familiar with the rules. It covers clinical studies operations, data management, and informatics, investigational product development and regulation, etc.

CRA

Junior Clinical Research Associates (CRAs) are introduced to Clinical Research, the life cycle of a clinical trial, how to monitor the clinical trial activities at different stages, clinical data monitoring, and management. It helps student become more familiar with the job of a CRA from the start of a clinical trial to its end. The course offered are similar to as those of a CTA’s.

Senior Clinical Research Associates (CRAs) are given opportunities to face more complex clinical trials and site management issues. The program will highlight the importance of international research as well as the role of the ICH GCP process. It also gives updates on the overview of current legislative requirements including:

• guidance on substantial trial modifications,

• improving the recruitment process of subjects and site staff

• how to prioritize and upgrade clinical trial monitoring tasks and activities

• accurate monitoring and reporting, dealings with non-compliance

• efficient tracking and coaching and mentoring junior CRAs

The courses offered will expand the knowledge and improve the monitoring skills to help take and make the right actions and decisions to resolve site issues.

Each of the courses is designed to produce competent clinical research professionals.

Take courses from CCRPS and learn more on how to become Clinical Trial Assistants, and Junior and Senior Clinical Research Associates.

Take courses from CCRPS and learn more on how to become a clinical research professional.

Here are some courses you might consider:

• Clinical Research Coordinator Certification - Ideal for those looking to coordinate clinical trial activities.

• Pharmacovigilance Certification - Focuses on drug safety and adverse effects management.

• CRA Certification - Prepares you for the role of Clinical Research Associate.

• ICH-GCP Certification - Essential for professionals needing to understand Good Clinical Practice guidelines.

• Clinical Trials Assistant Training - Provides foundational knowledge for those starting in clinical trials.

• Advanced Clinical Research Project Manager Certification - For experienced professionals aiming for project management roles.

• Advanced Principal Investigator Physician Certification - Tailored for physicians leading clinical trials.

• Medical Monitor Certification - Designed for those overseeing the medical aspects of clinical trials.

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Clinical Trial Protocol

Download our advanced review of the: Clinical Trial Protocol PDF

What is a Clinical Trial Protocol

Clinical trial protocols are the plans that are followed by all clinical trial professionals. They are designed to balance the benefits and risks of all clinical trials. The clinical trials are often sponsored by clinical trial sponsors who are responsible for the managing, initiating, and/or financing of clinical trials, but they do not conduct or supervise the clinical researches. Clinical trial sponsors include people, companies, government agencies, organizations, or other institutions.

What is the purpose of a Clinical Trial Protocol

The protocols are guidelines to answer specific research questions. They include the following; the goal of the study, the details on tests, treatments, and procedures, the eligibility of participants that will take part in the clinical trials, the length of the trial, the information needed and gathered, and protections against the risks to participants.

A clinical trial is always led by a Principal Investigator (PI), who direct members of the clinical research team regularly monitor the health of the participants to help determine and evaluate the safety and effectiveness of the study.

There are different types of clinical trials to you can work in, from which you can earn $60,412 - $160,876 a year.

1. Screening Trials: This trial tests new ways of detecting diseases or health conditions.

2. Prevention of Trials: This trial looks for the best way to prevent diseases from happening or reoccurring.

3. Diagnostic Trials: This trial studies and compares tests or procedures in the diagnosis of a particular disease or condition.

4. Behavioral Trials: This trial evaluates and compares ways to promote behavioral changes to improve health

5. Supportive Care Trials: This trial explores the new ways to improve comfort and quality of life for people with illnesses and conditions.

6. Treatment of Trials: This trial tests new treatments, a new combination of drugs, new drugs, new surgical procedures, new radiation therapy, and new medical approaches.

There are four phases of clinical trials which serve different purposes and help answer different questions.

Trials Phase 1. This is the testing of drugs or treatments within a small group of people ranging from 20 - 80 to study the drugs or treatments to learn and identify the side effects and safety of the drugs.

Trials Phase 2. This is the testing of drugs or treatments within a large group of people ranging from 100 - 300 to determine the effectiveness of the drugs or treatments and to further study its safety.

Trials Phase 3. This is the testing of new drugs or treatments within a large group of people ranging from 1,000 - 3,000 to monitor its side effects, its effectiveness, it's standards, and also to collect information on how the new drugs or treatments can be used safely.

Trials Phase 4. This is the phase where the new drugs or treatments get approved by the FDA and is made available to the public, to track its safety and to also seek more information about the benefits of the drugs and the treatments.

Learn More

Take courses from CCRPS and learn more on how to become a clinical trial professional with our training programs:

• Pharmacovigilance Certification

• CRA Training

• Clinical Trials Assistant Training

• Advanced Clinical Research Project Manager Certification

• Medical Monitor Certification

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A clinical trial is a branch of clinical research, which is a major component of medical research and it involves everyone including you. It consists of volunteers, doctors, and clinical researchers working together to learn more about diseases and how to improve health care for people.

Clinical trial includes the following branches:

• Behavioral: This branch improves the understanding of human behavior and how it relates to diseases and health. Enhance your expertise in this area with the Clinical Trials Assistant Training.

• Health Services: This branch focuses on the way people access health care services and service providers, how much health care costs, and the results of the care to the patients. Develop a deeper understanding by exploring our Advanced Clinical Research Project Manager Certification.

• Epidemiology: This branch focuses on improving the understanding of a disease by studying, the cause, patterns, symptoms, effects, prevention, and cures in specific groups. Our Pharmacovigilance Certification can provide you with the tools to better analyze these patterns.

• Clinical Trials: This branch helps evaluate the effects of an intervention on health outcomes. Get trained as a Clinical Research Coordinator to oversee these critical evaluations.

You must be wondering why you should be a part of the professionals that engage in clinical trials, right? Let's give you some insider scoop. Clinical trials are at the heart of all medical advancement around the world, and it provides one of the highest pay in all the medical field. Salaries range from $65,854 - $160,654. Clinical trials is important. It looks at new ways to detect, prevent, and treat diseases. Professionals study new medical devices, new drugs, new combinations of drugs, new surgical procedures, new ways to use existing treatments, new ways of behavioral changes to improve health, all to find new ways to improve the quality of life.

The main goal of all clinical trials is to determine if the detection, treatment, prevention, experimentation, and behavioral approaches to health care are effective and safe. Clinical trials offer hope for people with illness, diseases, or healthy volunteers receive new treatments and care as well as take part in finding new ways to help others.

Consider enhancing your capabilities with our CRA (Clinical Research Associate) course, ICH-GCP training, or the Advanced Principal Investigator Physician Certification to learn more about overseeing medical research studies. Additionally, for those interested in overseeing drug and device safety, our Medical Monitor Certification is available.

Take courses from CCRPS and learn more on how to become a clinical research professional.

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Clinical research courses are a prerequisite to any certification in the clinical research field. Clinical research is the investigation that is focused on determining the safety and efficiency of new medical products that includes; devices, diagnostic agents, vaccines, drugs, and treatment procedures that are intended to maintain, regain, and experiment new possibilities for human health.

Clinical research looks into the prevention, treatment, diagnosis, and relieving symptoms of diseases. They carry out medical investigations on healthy and diseased human volunteers to generate information that can be used to treat, diagnose, prevent, and curtail diseases and their symptoms. Clinical professionals develop, research, and test new applications in medical and clinical science, as well as develop new applications which include, medical procedures, vaccines, and pharmaceuticals to be tested in clinical trials.

So, what are the minimum requirements needed to study clinical research courses?

• Doctorate degrees (M.B.B.S, B.S.S.M, B.A.M.S, B.V.Sc., B.H.M.S, B.D.S, B.U.M.S.)

• Bachelor’s degree in Pharmacy or Physiotherapy (B.Pharm., M.Pharm.)

• Life Sciences (Biochemistry, Toxicology, Biotechnology, Microbiology, Botany, Zoology, or Pharmacology)

• Nursing

Taking these courses will open a lot of job opportunities in the clinical research field, as you can occupy any of the following posts;

• Clinical Research Associate (CRAs)

• Clinical Research Project Manager (CRPM)

• Clinical Research Programmer (CRP)

• Clinical Research Physician (CRP)

• Clinical Research Coordinator (CRC)

• Clinical Research Analysts (CRAn)

• Clinical Research Pharmacovililance

• Biostatistician, etc.

Since clinical research deals with the diverse experiments conducted with living organisms or humans, the major parts of the course will focus on the following;

1. The organic activities performed in the clinical trial sites.

2. The study of drugs and medicine management.

3. The manufacture of medicine and drugs

4. The study of related disciplines such as biochemistry, epidemiology, biostatistics, transplantation, etc.

5. The advanced study of the sub-specialties of data management, epidemiology, biostatistics, and research design.

6. The determination of the appropriate quantity and quality of drugs to be ingested or taken into the body, and the impact of it to the body, as well as the reaction of the body to the drugs.

All candidates that are enrolled into the course are expected to choose an area of specialization from the following:

• Genetics

• Epidemiology

• Patient-specific research

• Translational research

Since clinical research deals mainly with the research of medical equipment and medicines based on their safety and performance, it is one of the most important industries pertaining to the healthcare domain. Additionally, it is also one of the highest paying industries, with the average annual salary ranging from $56,984 - $156,678.

Take courses from CCRPS and learn more on how to become a clinical research professional.

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In the wide field of clinical research professionals, there are lots of job opportunities as well as job posts. They include; clinical research coordinators, clinical research project managers, clinical research trial managers, principal investigators, clinical research analysts, and many more. In this article, we will talk about the clinical research analyst position.

What does a clinical research analyst job entail?

Clinical research is often conducted and carried out in clinics, hospitals, clinical research trial sites, medical facilities, or laboratories (private and individual companies or pharmaceuticals). In effect, clinical research analyst work hand in hand with clinical research professionals within the medical field. They work on medical studies designed to measure the effectiveness of a medical device, drug, or medical process on the human body.

A clinical research analyst directly works under clinical research management. They work within teams that conduct medical studies, clinical research, and clinical trials.

Clinical research analyst are one of the many key players in clinical trials and medical studies. They combine clinical sciences, scientific research, medical education, analytical and communications skills, and sometimes financial skills and knowledge to their job. Their role is very flexible. They can be in labs, directly working with patients, or they can be providing scientific or financial insight to physicians and principal investigators.

The general job description of a clinical research analyst includes the following;

1. Working with scientists or physicians who oversee the clinical research process and procedures.

2. Direct interaction with patients by interviewing and screening them as potential candidates.

3. Collecting data from the clinical trial sites for further and accurate study.

4. Carry out research accounting and budgeting, this is where their financial acumen comes into play.

5. Acting as liaisons between supervising physician investigators and other medical staff such as nurses.

6. Coordinating clinical research studies by tracking inventory, collation, and collection of data, identifying and interacting with patients, and overseeing protocols.

7. Acting as the primary financial resource to go to for clinical study.

To be a clinical research analyst you need to have a minimum of an associate’s degree for an entry-level qualification. You will need a bachelor’s or master’s degree for higher level positions. For a clinical research analyst, work experience in a clinical research setting or other clinical related field is a requirement.

The prospective job growth is promising, as it is projected at an estimated 16% growth till 2024, with an estimated annual salary of $60,520 and above.

Take courses from CCRPS and learn more on how to become a clinical research professional.

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Clinical trial managers are one of the most important roles when it comes to the development of new medicines. They ensure the safety of the human subjects that are involved in a clinical trial. Apart from that, they also weigh and validate the outcomes of the trial against industry standards. Do you like the idea of being a clinical trial manager? Then here’s how to become a clinical trial manager.

The steps are quite simple. In preparing to become a clinical trial manager, you should obtain a bachelor's or master's degree in clinical sciences, life sciences, or other health sciences related fields. Get a post-baccalaureate certificate from CCRPS, and get administered by the Academy of Clinical Research Professionals.

A good clinical trial manager course should include enrollment into at least 6 required courses (site management, good clinical practices (ICH-GCP), drug development procedures, clinical research writing, and statistical analysis) and 1 elective to earn your clinical trial manager certification. You are also required to take some computer science courses to have knowledge of Clinical Trial Management System and Oracle Clinic, programs you will need to know for the job.

This job entails receiving accurate information, decision making, and problem-solving organizing skills. This means that you must be familiar with planning, work updates, establishing interpersonal relationship skills, and maintaining interpersonal relationships.

As a clinical trial manager you tend to be a working manager for smaller staff (this makes you a part of the research process). However, you could be a working manager with larger staff (this makes you stay in a supervisory role). Whatever the case might be, CTMs coordinate the activities of their unit with other units and makes sure that the financial, production, and marketing specialist are fully equipped with supplies, equipment, and materials. They are in charge of directing the activities related to the research, development, and coordination of clinical trials.

As a CTM you will:

• hire, supervise, and evaluate technicians, staff members, and scientists

• ensure that the laboratories are fully stocked and equipped with supplies and equipment

• provide technical support to scientists and technicians

• monitor the progress of projects

• draft out operational reports

• review all performed research and

• report all researched results accurately

• establish and make sure that administrative procedures, standard, and policies, are duly complied to and followed

• direct and coordinate the development of project products, production activities, and scientific research activities (improving the process of manufacturing)

The average salary earned is between the range of $100,289 - $150,874, though that may vary based on location. Job boards are a great way to check on positions available near you.

Get a course at CCRP and get certified to become a Certified Clinical Trial Manager.

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The curriculum and syllabus are important parts of any education and training programs for clinical research professionals. Thus, they help determine the structure and quality of international educational services around the world.

One of the foremost international educational services institutions is Barnett International. Barnett International was founded in 1979 and is widely known for its educational courses, training consulting services, and training programs for clinical research professionals all around the world.

Clinical research training platforms vary depending on the learning requirements. Barnett International offer training, interactive web training sessions, and e-learning modules for specific clinical research roles. They provide students with a training experience that is uniquely focused on core competency development. Their clinical training curriculum covers Clinical Research Coordinators (CRCs), Clinical Research Associates (CRAs), Principal Investigator (PIs), Clinical Data Managers, Regulatory Affairs, Clinical Quality Assurance, Clinical Project Managers, and other clinical research roles. Most importantly, heir courses provide the flexibility and engagement for every kind of student.

For those looking to specialize further, consider enhancing your skills with specific courses such as the Clinical Research Coordinator course or the CRA training offered by CCRPS, designed to meet the needs of individuals aiming at these roles.

We can take a look at another international educational service institution, which is the Institute of Clinical Research (ICR). ICR is perhaps the oldest international educational service provider for clinical researchers. They are known for providing high-quality training, support, and networking to the clinical research community.

How do they achieve all this? The ICR strives to support their members throughout all the stages of their careers by defining and refining standards for the clinical research industry. They do so by providing an interactive forum where the discussion of key issues that affect and impact clinical research takes place.

They also provide opportunities for learning and development to enhance the competence of clinical research professionals. Clinical professionals that know what they are doing boost the public confidence, outlook, and understanding of clinical research as well as promote a good relationship with other healthcare related professionals.

CCRP is another international educational services provider that is known for their clinical research online training for every student. Courses like Pharmacovigilance Certification and ICH-GCP training cater to those interested in ensuring safety and compliance in clinical trials. The Advanced Clinical Research Project Manager Certification and Advanced Principal Investigator Physician Certification are ideal for those looking to ascend to higher roles within the field. Furthermore, the Medical Monitor Certification offers specialized knowledge for overseeing clinical trial safety.

CCRP courses are accredited by the ACCRE and curated by real life professionals that know what information is most important for a student to learn. The training course are self-paced and online. That means you can take the course on your own schedule and learn how you learn best.

The goal of these international educational service providers is to ensure and support excellence in clinical research. By implementing competent members with the training, certification, and development tools, their student can work ethically, responsibly, and professionally anywhere in the world.

Become a part of clinical research professionals and see yourself earning $81,654 annually on average. Researching jobs positions near you can give you a better idea of what is available in your location. Want to get started? Check out our website and let us help you succeed.

Take courses from CCRPS and learn more on how to become a clinical research professional with our Clinical Trials Assistant Training.

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The purpose of the clinical research seminars is to impact the attendees with knowledge about important aspects of clinical research, such as the professional ethics, operational aspect and regulations. Education and training are very important in this field and vital to the success of trials. Seminars are another way of training clinical research professionals or other related professionals that have an interest in the field.

Seminars can be held every two weeks, monthly or quarterly. It depends totally on the organizers and what they aim to achieve with the seminar. For example, some organizers may hold a biweekly seminar for young interns to help them improve their knowledge and sharpen their clinical research skills.

Clinical research seminars are ideal for the following sets of people:

• Clinical research coordinators

• Project managers

• Nurses

• Clinical research associates (CRAs)

• Regulatory experts

Other staff also involved in clinical research can as well attend the seminar to improve their knowledge. Common topics that are discussed at the seminars include :

• Good Clinical Practice (GCP)

• Professional ethics of clinical researchers.

• Auditing clinical trials

• Advanced quality monitoring

• Monitoring oncology trials

• Current regulations

• Inspection preparation

• Resources involved with clinical research.

• Guidelines pertaining to clinical research.

These seminars are usually handled by experts and professionals in the clinical research industry. They are usually have worked with different leading pharmaceutical companies biotechnological companies, device companies, and leading academic institutions.

Clinical research seminars can also provide extra benefits. This depends a lot on who the organizers are, but some clinical research seminars provide those in attendance with SOCRA (Society of Clinical Research Associates), ACRP (Association of Clinical Research Professionals) and CME Continuing Education Credit hours.

Apart from seminars organized by different institutions that an individual can apply for, seminars can also be organized for in-house training. They can be tailored to meet your company's specific needs. Organizers can provide your company with a set of training options that range from single topic seminar presentation to more comprehensive programs. For instance, some organizers make use of different hands on approach by providing activities and simulated case studies to help the audience's learning process.

As an individual you can register yourself to become a participant of upcoming clinical research seminars at ccrps.org. As an organization or company as well, you can register your staffs for these seminars. As a company, you can register for in-house training, where the seminars can be tailored for your specific needs.

Take courses from CCRPS and learn more on how to become a clinical research professional.

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Clinical research plays a very vital role in medical health care. Before anything is put into practice, it will have to be discovered first and tested: this is the role of clinical research.

Free online courses on clinical research teach the basics of clinical research. They help students understand more about modern health care and the role of clinical research and its discovery. Courses like these are ideal for college students and people who are considering taking up a career in health care and life sciences. It is also good for social care practitioners that want to find out more information about the role of clinical research in improving the quality of healthcare.

Clinical research training for research professionals include taking necessary courses and getting the necessary accompanying certification. However, clinical research professionals can also take part in courses teaching the rudiments of clinical research and good clinical practice. An example of one of such courses is the one offered by National Institutes of Health (NIH). The course "Introduction to the principles and practice of clinical research" is a course that teaches professionals how to improve their effectiveness and to as well safety. This course covers topics like study design, monitoring and regulatory considerations, how to prepare and implement clinical studies, statistics, ethical and legal considerations in clinical research, measurements, additional study design etc. A course like this helps you to understand the very basics of clinical research and improves your efficiency.

As good as free online clinical research courses are to help you develop your career as a clinical research professional, they are not meant to take the place of the required training needed, especially those that train you in the protection of the human subjects of clinical research. For those interested in specializing further, consider the Advanced Clinical Research Project Manager Certification or the Advanced Principal Investigator Physician Certification.

For further details and information on how to get free online courses for clinical research professionals, visit ccrps.org. Whether you are a research professional looking to learn more and better your career or you are a student or someone just taking up an interest in the field of clinical research, there will be something for you.

Take courses from CCRPS and learn more on how to become a clinical research professional, such as the Clinical Research Coordinator, Pharmacovigilance Certification, CRA, ICH-GCP, Clinical Trials Assistant Training, or Medical Monitor Certification.

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Clinical research associate training is the grooming of clinical researchers to become associates. It's a promising career in the clinical research industry. Any worth-while training will include everything you need to know to about the job and become one of the best.

Clinical Research Associates are those responsible for the planning, setting up, and coordinating clinical trials. They provide technical assistance for experiments, make sure that the scientists that are involved in the clinical research trials comply with regulatory standards, and also collect results during the clinical trials. When the trials are over they are also to be involved in the presentation of the results to the public in a manner that is useful and understandable. Enhance your skills as a Clinical Research Associate with CRA training.

The amazing part about being a clinical research associate is that jobs are available in both the laboratory and office setting.

To be an associate in clinical research you need a minimum degree of a bachelor's or master's degree in the clinical research field of study or a related field. They have the key responsibilities of designing and implementing clinical research trials, to train staff, to monitor progress, to screen test subjects, to present findings, and to help maintain the database of all clinical research trainees.

The median salary of a clinical research associate boasts of $61,932 annually. It is one of the most attractive salaries for someone with a science degree, as it is always on a rise and there is always a ready market for clinical research professionals.

A clinical trial is a method in which new medical treatments and pharmaceuticals are developed and experimented and this is where clinical research associates come in. They are an integral part of the process, as they work with teams to design, implement, and organize research trials to test out the effectiveness of the proposed medicines on humans. They are responsible for the different parts of clinical trials which include, training of staff, screening test subjects, monitoring the progress of staff, present findings, and maintain the database. Communication skills, science knowledge, and a strong mathematics knowledge base are the core skills you need in the clinical research profession. For those interested in more specialized roles, consider the Advanced Clinical Research Project Manager Certification or the Advanced Principal Investigator Physician Certification.

You can come from a variety of medical sciences or health-related fields, such as a nursing background as an RN. Courses offered expand on clinical related ethics, team management, and research methodologies.

CRA training certificate examination comes with one of the three combinations of education and experience.

• High school diploma and 6,000 hours of experience.

• An associate degree in clinical research fields and 4,500 hours of experience, or

• A Bachelor's, Master's, or Registered Nurse degree and 3,000 hours of clinical research experience.

Get a clinical research associate certificate from certified clinical research professionals course, and earn your way to one of the most lucrative fields in clinical research. At CCRPS, we support online learning, so you can take the classroom everywhere. Learn more about Clinical Research Coordinator training and Pharmacovigilance Certification to broaden your expertise.

Take courses from CCRPS and learn more on how to become a clinical research professional. Further your understanding of good clinical practices with the ICH-GCP course.

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Clinical research coordinator (CRC) play an integral role in all kinds of medical studies. Working under the direction of the principal investigator, who designs, conducts, and manages clinical trial; the clinical research coordinator supports, organizes, and facilitates the daily activities of the clinical trial.

A Clinical research coordinator manages, oversees, executes tasks and day to day clinical trial activities. They also work in conjunction with sponsors, departments, and institutions to manage finances, obtain compliance, and work through personal issues.

Their responsibilities include the planning and management of the following initiatives:

• study

• enrollment

• maintenance

• training

• compliance with institutional, state, and federal regulations

CRCs engage directly with the trial participants, screening them for eligibility. They also help develop and implement recruitment strategies and work with all the available teams during the trial period.

In the lab, CRCs carry our experiments, medical studies, and clinical researches. A CRC works closely with labs, medical centers, and research hospitals to evaluate research protocols and seek approval from regulatory committees.

To get certified as a CRC, you must have either:

• A bachelor's or higher degree in health sciences in clinical research administration and submission of a fully detailed resume that documents at least 3,000 hours of performed designated duties

• A Registered Nurse (RN), LVN, Licensed Practical Nurse (LPN), or an associate degree and a submission of a detailed report that documents at least 4,500 hours of performed designated duties.

• Worked as a laboratory technician, medical assistant, or a high school diploma and submission of a detailed report that documents at least 6,000 hours of performed designated duties.

For those with a bachelor’s, a degree in medical technology, public health administration, or microbiology, with an additional two years master's degree in management positions (optional) is ideals. Human anatomy, biostatistics, epidemiology, health care management, biochemistry, and mathematics, are the courses typically required for these majors.

Management and communications experience coupled with interpersonal and multitasking skills are essential job skills to possess. Internships and/or low entry-level jobs as health care workers or lab technicians should also be considered to get familiarized with the working environment. It is important to note that there may be a substitution for hours of qualifying work experience.

After qualifying, you need to pass an exam and get certified. A CRC certification lets you practice legally and can see you earning from as little as $48,000 to as much as $60,000 annually.

To learn more, take a course in clinical research coordination to help develop and refine your skills before you go on to get the clinical research coordinator certification.

Discover more from Clinical Research Training | Certified Clinical Research Professionals Course. Other recommended courses for aspiring professionals include:

• Pharmacovigilance Certification

• CRA Certification

• Clinical Trials Assistant Training

• Advanced Clinical Research Project Manager Certification

• Advanced Principal Investigator Physician Certification

• Medical Monitor Certification

These courses provide essential knowledge and training for those interested in advancing their careers in clinical research.

Take courses from CCRPS and learn more on how to become a clinical research professional.

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A Master's in Clinical Research opens up a wide range of job options. There's a huge market for clinical professionals with experience and expertise in the developing, conducting, and monitoring processes in clinical trials to help transform scientific discoveries and research into possible and usable treatments.

It's a dynamic, high demand profession that fits all lovers of science. Getting a Master's in Clinical Research gives you the skills to develop, conduct, coordinate and monitor clinical studies. It also helps you comply with the protocols of regulatory agencies.

A Master's in Clinical Research can take you to more financially rewarding clinical research career choices and opportunities. It can also set you up to work at a variety of companies, like public and private medical institutions and companies, contract research organizations, hospital systems. Once you are in the field, there is an enormous amount of position choices. Additionally, you can expect a steady promotion to industrial, research, managerial, supervisory or specialist positions.

The minimum requirements you need for your Master's in Clinical Research are either a bachelor's degree in medical sciences, an advanced education in health professions with work experience, or a standardized test score like GREs.

Clinical research masters online will include a combination of the following;

• Regulatory and compliance issues

• Biostatistics and computing

• Epidemiology

• Clinical research trials designing

• Medical informatics

• Health services research

• Supervised clinical research

• Concentration in research management

• Patient-oriented research

• Experiential learning in clinical research

• Clinical trial management

• Concentration in investigation

• Regulatory affairs

• Conducting clinical research studies

• Health care

• Biologics

• Health sciences policies

• And others

A Master's in Clinical research is a 30 - 33 credit program, depending on the course you want. It is comprised of required courses, program electives, course works, cognate electives, thesis or project, and supervised research. There's a wide range of specialized clinical research masters to go for: clinical research professional, clinical research administration, clinical research coordinator, and others. As an area of medical sciences that is growing tremendously. Demand is so high that the median salary is $82,090 and varies depending on the geographical location and work experience. You can check positions and salaries near you here.

To learn more about the courses offered and how the Master's in Clinical Research program is run, check out this clinical research master's degree program.

Take courses from CCRPS and learn more on how to become a clinical research professional.

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Clinical Research Training For Employers

No employer in any field or industry employs a staff without a prior knowledge, ability or competence in carrying out their supposed duty and fulfilling their job description. It is the same with the clinical research industry as well. Examples of employers in this industry are pharmaceutical companies, biotech companies, clinical research organizations, government agencies etc. These companies and organizations all require a minimum level of training that individuals must possess before they can be considered employable. There are minimum educational requirements, certification and certain other skills that employers consider before employing a clinical research professional.

However, because of the nature of medical science, the growth and evolution of science and the advancement of technology, here is a constant need for clinical research professionals. This has increased the importance of clinical research training for employers.

Employers who want to increase the level of professionalism and competence among their staffs often enroll them for online and offline training programs. There are different variations of these programs, depending on the training platform. Some of these variations offered by different platforms include:

• Classroom training: this program reduces the amount of time spent out of office or work by the staffs. In this program, the trainers come down to the company's facility to train the staffs. This reduces the amount of time the staffs will spend traveling, as well as the travel expenses. This increases the staffs competence and improves their job performance while at work.

• Online training: this is a convenient and self-paced electronic based training program that makes use of different adult learning techniques that enables the students (organization's staffs) to fully understand what has been taught. This makes it easy for them to apply what they are learning on the job. This program makes use of different online platforms that ensures interaction between the lecturers and the students. For comprehensive online training, consider courses like the Clinical Research Coordinator, Pharmacovigilance Certification, and ICH-GCP from CCRPS.

• Custom program: this program allows the team of trainers to work with the organization's staffs in order to develop online and offline training programs that are tailored to meet the needs and specifications of the organization and its staffs.

• Boot camp and onboarding program: programs like these are most usually for clinical research associates and clinical research coordinators. The onboarding program is ideal for new CRAs. It is a unique intensive training program that can be customized to meet the company's needs. These programs allows the new CRAs and CRCs to make immediate impact and saves the organization more time and money. Specialized training for CRAs and CRCs can be found through the CRA Training and Clinical Trials Assistant Training at CCRPS.

Take courses from CCRPS and learn more about how to become a clinical research professional. Advanced certifications such as the Advanced Clinical Research Project Manager Certification and Advanced Principal Investigator Physician Certification can significantly enhance the expertise and capabilities of your team. Additionally, for those in more specific roles, the Medical Monitor Certification is also available.

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The role of the clinical research associate is very important in clinical trials to ensure that medical devices, new treatments and new drugs are approved for patients' use.

This field is taken as a certificate program course in many schools. You may also discover the availability of associate degree programs depending on the school. These programs can be completed in two years and can be offered through both the online and the hybrid formats. Hybrid formats combine both online and on-campus courses together.

If you opt for an online program, different platforms like emails and discussion boards are used to ensure and promote interaction between the students as well as with the lecturers. Online learning platforms are used to upload the syllabus, course materials, lectures and assignments. Some online programs include field work as part of their requirements, in order to gain first hand experience working with clinical trials and patients. Depending on the school, they may have a list of approved clinical research institutes and other facilities. Otherwise, you will have to find a facility for yourself and get the school's approval.

These certificate programs are generally designed for professionals that are already in the medical fields like medical assistants, nurses etc, and are interested in moving to the field of clinical research. They may therefore ask for a copy of your CV or resumé or they may ask for a letter from your employers to verify that you have the needed medical experience. Some programs may require just an undergraduate degree in a medical science or life science related field.

Clinical research associates are trained to assist clinical researchers and investigators in the coordination, administration and management of clinical trials. During this training, different courses will be taught revolving around subjects like safety procedures, subject recruitment, regulatory requirements, drug development, accountability, trial management, medical terminology etc.

The importance of the role of the clinical research associate means that companies that conduct clinical trials are usually very selective, the need to comply with strict regulations often inform their decision when making a choice of their clinical research associate. It is therefore very difficult to get a job as a clinical research associate without previous experience of clinical trials. Many companies require around at least two years experience in clinical monitoring as a clinical project assistant or clinical trial administrator before considering applicants for this important role.

In applying for the post of a clinical research associate, ensure that you read the job description and indicate or highlights the relevant experience on your curriculum vitae. Your cover letter should be specific to the company you're applying to. Do not use a one-for-all cover letter. Personalize your cover letter to each company and highlight the skills that fit the specific requirements of the role. Not all companies advertise their vacancies, so you can try to find out about other unadvertised vacancies.

Take courses from CCRPS and learn more on how to become a clinical research professional. Explore courses like Clinical Research Coordinator, Pharmacovigilance Certification, CRA, ICH-GCP, Advanced Clinical Research Project Manager Certification, and Advanced Principal Investigator Physician Certification.

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The work of a CTA (clinical trial/research assistant) is one of extreme importance to the clinical research institute. CTAs work in a very busy department. To succeed, they needs to have a keen eye for details and an open mind to learn. They need to be able to ask the right question and find the right solutions.

DUTIES

The CTA helps in the collection and organization of data that is procured from studies. A typical day of a CTA is spent observing and communicating with the volunteers who are recruited to handle these kinds of studies. They are then responsible for analyzing and interpreting the statistics, which helps researchers realize their conclusions and results.

One of the critical tasks of a CTA is performing the different safety and quality checks within their unit. These checks are routinely carried out daily, weekly, or monthly. For example, standard equipment such as freezers and fridges are checked at least twice daily. This is important because they are used for storing samples and medications that needs to be kept in controlled temperature. Even a slight deviation from the controlled temperature can impact the validity of the result and the research.

Additionally, emergency equipment is checked on a daily basis. This ensures the safety of all the staffs and volunteers within the clinical research institute.  

Another part of a CTA's job is to assist members of the team and deal with queries from members of the public. A CTA has to work in an administrative capacity and help with research paperwork. There are others who may have to perform some basic medical responsibilities like administering the medication for trials and even drawing blood.

In the midst of these many duties, it is very important that the CTA is good at multitasking. A good communication skill (both written and verbal) is also very important in this line of work.

EDUCATION

Most of the jobs in this area need a person to have a bachelor’s degree within the life sciences. However, there are some employers who require an advanced graduate degree, like a BMSc.

It is important for the clinical research assistants have a strong educational background in the administration of clinical trials. This means that you may have the kind of skills that help in organization. Having an interest in statistics and math can be an added advantage.

If you don’t have a degree in the science field and don’t want to go back to school, finding training and real experiences in clinical trials is going to help you hand a CTA position. At CCRPS, we offer effective courses and experiences you need to get your foot in the door. We have a CTA course and a free ICH GCP certification course, which teaches important skills that will help you succeed in clinical research. If you are looking to advance further, consider our Advanced Clinical Research Project Manager Certification or the Advanced Principal Investigator Physician Certification. For those interested in the crucial aspects of drug safety, our Pharmacovigilance Certification might be the right fit. Explore these to gain deeper insights and practical knowledge.

Take courses from CCRPS and learn more on how to become a clinical research professional.

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With scientific discoveries and technological advancements comes knowledge. This knowledge defines the scope and practices of the different fields of professions that they apply to. Due to the continuous nature of medical research, the medical sciences are not also behind on scientific discoveries. More often than not, there is a new field knowledge that changes the way people do their job. The change could be something in something routine as checking the blood pressure of a patient or measuring the body temperature. A smart clinical research scientist knows that they have to ensure that they stay up to date with scientific discoveries to help patients as well as themselves.

If you have been offered a clinical research job or you are interested in one, one thing you should know for sure is that to be successful in this field, you need to know your stuff. It is true what they say, to remain relevant in any field is to remain knowledgeable.

To help your cause, we have made a list of 6 books that will help you succeed in the clinical research field.

• Fundamentals of Clinical Trials, by Lawrence M. Friedman, Curt D. Furberg, David DeMets. This book looks into key issues like assessment, reporting of results, randomization, interpretation etc. This book introduces clinical trials to you beautifully, with real life examples used to explain key features of clinical trial.

• Designing Clinical Research, by Dr. Stephen B Hulley, MD, MPH, Steven R Cummings, MD, Warren S Browner, MD. This book is an important book for doctors, pharmacists, nurses and all medical professionals involved in medical research. It explains useful methods for designing, funding and implementing clinical research.

• Publishing and Presenting Clinical Research, Third Edition, by Warren S. Browner MD. This book contains the essentials of clinical trials and publication. This book will come in handy for those who wants to know more about organizing, delivering, and publishing the results of their research in the best way possible.

• Practical Guide to Clinical Data Management, Third Edition, by Susanne Prokscha. One issue that always pops up in clinical research is how to manage the large volumes of ever increasing data. If you are already working in the field, you could no doubt relate. This is a task that can be rightfully described as “extremely time consuming”. This book gives powerful insights on current industry tactics on the use of Electronic Data Capture (EDC) for clinical research. This book will help you solve the age-long problem of managing voluminous clinical research data.

Honorable mentions

• Basic Principles of Clinical Research and Methodology by S. K. Gupta

• A Clinical Trial Manual from the Duke Clinical Research Institute. Kate Davis, Margaret Liu.

• Handbook for Good Clinical Research Practice. WHO.

We have introduced many good reads for those who like to stay informed. Whether you are someone looking to get started in the field or someone who is looking for a refresher, these are the perfect places to start. If you need motivation to get reading, here are some clinical research positions to remind you of what is possible when you apply yourself.

If you prefer online classes with professional guidance, check out CCRPS’ certification courses. They offer one of the only major ACCRE accredited courses in the US. The courses are created by real, senior professionals who skip the nonsense and get right into what you need to succeed in the field.

To learn more about the role of a Clinical Research Coordinator, consider this Clinical Research Coordinator course.

• Explore the realm of drug safety with our Pharmacovigilance Certification.

• Dive into clinical research specifics with the CRA certification.

• Understand the essential regulations with the ICH-GCP course.

• Begin your journey in clinical trials with the Clinical Trials Assistant Training.

• Enhance your skills with the Advanced Clinical Research Project Manager Certification.

• For physicians aiming at leading research, consider the Advanced Principal Investigator Physician Certification.

• Specialize in monitoring clinical trials with the Medical Monitor Certification.

Take courses from CCRPS and learn more on how to become a clinical research professional.

Discover more from Clinical Research Training | Certified Clinical Research Professionals Course

Clinical research billing is a very important part of medical research, but it is a little bit complex because there are usually more than one person involved or responsible for the bill or cost of a research.

There are three ways the billing of a clinical research can play out:

• When the procedures and services of a clinical research is solely for study purpose, the bill is generally cleared by the research sponsor. Those interested in managing such responsibilities can benefit from our Clinical Research Coordinator course.

• When the procedures and services of the research is considered to be a standard of health care or routine treatment and would have been administered to the subject even if there was no research. In this case, the bill is generally on the subject or the subject's insurer but the sponsor can be involved in the payment depending on contractual agreement. To understand the pharmacological safety aspects involved, consider our Pharmacovigilance Certification.

• There are those that are a mixture of both. Procedures that are standard treatment billed on the subject and their insurer and procedures that are solely for research purposes billed on the research sponsor. To learn more about handling these scenarios, check out the Advanced Clinical Research Project Manager Certification.

Depending on contractual agreement between the research sponsor and the subject of the research, treatment of adverse effects of the study might be paid for by either the sponsor or the subject (and their insurer). Those interested in managing clinical trial processes may find the CRA course useful.

Due to the number of parties involved in the billing process, there could be some miscommunication and it could lead to billing errors. It is important to note that the clinical research centres have financial regulations to comply with, like the clinical research billing compliance. They guard against financial issues that may occur like double billing. Our ICH-GCP course can provide insights into these essential guidelines.

For instance, if a research has already been paid for by the sponsor, it must be communicated to the clinical research institute so that they don't bill the subject (patient) or their insurer. If the subject is billed for a research paid for by the sponsor, that is called double billing and an obvious transgression against clinical research billing compliance.

The exception is in cases where there's a legal contractual agreement for both parties to be responsible for the payment. This is possible in a situation like the third scenario above, where there is a mix of procedures for standard treatment and procedures for research purposes. The sponsors can clear the bill for the procedures that are solely for research purposes while the subject and their insurer is billed for the procedures that are standard treatment. Communication between concerned parties is key in clinical research billing.

Another common compliance risk is to charge a subject for a procedure that was promised as free in the research informed consent form. Every promise made to the subject in the form must be kept. Enhance your skills in this area with our Medical Monitor Certification.

To learn more, you can take a course in clinical research billing compliance. This will help develop your knowledge and skill in maintaining compliance and other practices involved with clinical research billing.

For those looking to specialize further, consider the Advanced Principal Investigator Physician Certification or begin your journey with our Clinical Trials Assistant Training.

Take courses from CCRPS and learn more on how to become a clinical research professional.

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$40,000If an agency requires 20% cost sharing of the total project for a particular program and a proposal is requesting $200,000 from agency, what is the additional amount that the institution must cost share?2.$50,000An investigator on a NIH grant has permission to rebudget $50,000 in supply monies into equipment. If the Institution's facilities and administrative cost (indirect cost) rate (based on MTDC) is 50% how much money will be available for the equipment3.$100,000An anti-lobbying certification is required on federal grants, cooperative agreements, and contracts exceeding a MINIMUM of4.$165,000An institution has an indirect cost rate of 40%. A research project is budgeted at $125,000 in direct costs including an item of equipment at $25,000 which is the only item excluded from the indirect cost base. What is the total cost for the project?5.1.Publicly known information.2. Already known information.3. Information received from others. 4. Information shared with others. 5. Independently developed information. 6. Information not included in the nondisclosure agreement.What is not included in a Nondisclosure Agreement?6.1) Resubmit 2)Appeal 3)Advice to look for other opportunitiesWhat happens to a proposal if it isn't funded?7.2NIH limits how many resubmissions on proposals?8.2 CFR 215 OMB A-110Administration Regulation for Education Institutes, Hospitals, and Non profits9.2 CFR 220, OMB Circular A-21Deals with cost determination but does not identify the circumstance or dictate the participation in the financing of a project

10.2 CFR 225 OMB A-87Cost Principles for State, Local, and Indian Tribal11.2 CRF 215 (OMB Circular A-110) provides regulations governing which of the following for educational institutions?
a. Administrative requirements for contracts
b. Administrative requirements for grants and cooperate agreements
c. Cost principles for grants and cooperative agreements only
d. Administrative requirements and cost principles for grants and cooperative agreementsb. Administrative requirements for grants and cooperate agreements12.3 years from submission of final report of expendituresRecipients of federal grant funds must retain records for a MINIMUM of13.5 membersAn IRB is required to have at least:14.6-9 monthsThe National Science Foundation indicates decisions on the funding of grant proposals should normally take15.26%The administrative cap on federal negotiated F&A rates is equal to16.90Under Expanded Authority, pre-award costs up to _____ days prior to the effective date of the award the PI can accrue charges before the award start date.17.90 daysIf final financial reporting (FS 425 Report) to federal agencies is not completed with in the typical ___ days, the institution is out of compliance18.90 daysWhen granted expanded authorities, pre-award costs on a federal grant may be incurred by an institution within a MAXIMUM of how many days prior to the official start date?19.90 daysHow many days do recipients of federal grants funds have to submits final reports after completion of the project?

20.A-102State and local governments are subject to which of the following OMB Circulars?21.AbstractShould be 5,000 to 25,000 words in length. This summary should demonstrate to the reader the most important parts of each of the sections of the research proposal in around 200 words.22.Accept, Decline or NegotiateWhen an award is made an institution has the following options.23.Access to federally funded research data is required under the:
a. Solomon Act
b. Davis-Bacon Act
c. Shelby Amendment
d. Stevens Amendmentc. Shelby Amendment24.According to federal regulations, which of the following must be included in an Institution Review Board?
a. Ethicist
b. Attorney
c. Member of the clergy
d. Member unaffiliated with the institutiond. Member unaffiliated with the institution25.Acquisition of property or servicesA procurement contract is used for the purpose of26.Administrative requirements for grants and cooperative agreements only2 CFR 215, OMB Circular A-110 provides regulations governing which of the following for educational institutions?27.AdobeWhat is required to use Grants.gov28.advise student to apply to the federal agency to request a proposal 90 days after proposal was submittedIf a graduate student comes into a university sponsored research office claiming that because of the federal Freedom of Information Act (FOIA) he has the right to obtain a copy of a recently submitted proposal, the research administrator should

29.Allocable costA cost that can be assigned to a project or an activity based on the relative benefits received30.allowable only if approved by the sponsoring agencyAccording to OMB Circular A-21, costs incurred prior to the project start date are:31.All vertebrate animalsThe Federal Animal Welfare Act applies to which of the following animal species32.AnnuallyIf an institution of higher education is subject to OMB Circular A-133, when must it have an independent audit?33.The Anti-Kickback Act of 1986Which of the following aims at deterring subcontractors from making payments and contractors from accepting payments for the purpose of improperly obtaining or rewarding favorable treatment in connection with a prime contract or a subcontract relating to a prime contract?34.An anti-lobbying certification is required on federal grants, cooperative agreements and contracts exceeding a MINIMUM of:
a. $100,000
b. $500,000
c. $1,000,000
d. 10,000,000a. $100,00035.approval of student's embassyIn order for a foreign national doctoral student researcher to work on a federal grant in an American institution, it is necessary for the student to have36.Assure that the highest quality proposals are selected for funding in an equitable mannerWhich of the following is the primary purpose of federal proposal review processes?37.An award similar to a grant, and anticipates having substantial involvement in research activities once the award has been made.What is cooperative agreement?38.Award terms and conditionsA Notice of Award typically includes which of the following

39.Basic and containment procedures designed to protect personnel and the environmentWhich of the following best describes essential laboratory biosafety levels in medical research?40.Bayh-Dole ActWhich of the following was enacted as a uniform patent policy among the many federal agencies that fund research?41.BequestsA type of donation or gift with few or no conditions specified. Gifts may be provided to establish an endowment or to provide direct support for existing programs.42.Break refreshments at a project sponsored workshopUsing the criteria contained in 2 CFR 220, OMB Circular A-21, which of the following costs would most likely be allowable as a direct expenditure item on a federal grant?43.Budget period is yearly. Project period is the life of the contract.What's the difference between budget period and project period?44.a cabinet-level departmentThe Office for Human Research Protection is administered by45.A career development programAn employee in a position which does not enable realization of full potential would benefit most from46.cash flow statementAn important tool you may use to measure and track the flow of
cash into and out of your operation47.Certifications and representationsJust-In-Time initiatives postpone the submission of which of the following items until a decision to make an award is reached?48.Change in allocation within a single budget categoryWhich of the following changes does not require prior National Science Foundation approval?49.Change OrderA written order signed by the contracting officer, directing the contractor to make changes that the changes clause of the contract authorizes the contracting officer to order without the consent of the contractor.50.Chief Executive Officer or Vice President of ResearchWho appoints the chair for each committees at universities

51.A citation of the contract clause authorizing the terminationWhich of the following information must be included in the notification by a federal officer to the contractor to terminate a contract for convenience52.Clinical trial AgreementWhich of the Following types of documents is most appropriate for testing the efficacy and safety of a new drug, device, or vaccine?53.Code of Federal RegulationsThe following provides information on patent rights and responsibilities currently applicable to universities and federally sponsored projects54.cognizant agencyA Federal agency responsible for negotiating and approving facilities and administrative cost rate for an education institution on behalf of all other federal agencies is referred to as the55.Commons Business DailyWhich of the following sources is not commonly used for federal funding opportunities?56.Compliance approvalsRetention of which records are required by the OMB57.Contact legal, then contact program officer over concernsIf a PI received an award and his wife is using the lab and charging to the award. How would you handle it?58.The contractor fails to perform the services within the time specified or any extensionWhich of the following is a reason for a federal contracting officer to send a "Show Cause" notice to a contractor?59.Contract Work Hours and Safety Standards ActThis act would require that certain contracts contain a clause specifying that no laborer or mechanic doing any part of the work contemplated by the contract would be required or permitted to work more than a certain number of hours in any workweek60.control commodities and is governed by Department of CommerceIn Export Control, what does Export Administration Regulation control and who governs it61.control money: Governed by Department of Treasury.In Export Control, what does Office of Foreign Assets Control control and who governs it

62.Cooperative Research And Technology Enhancement Act hopes to enhance research among Universities, private and public sectors, by treating joint inventions as if they are a single owner but only if the collaborators sign an agreement prior to the invention being created.What is the CREATE Act?63.CopyrightIn which of the following areas of intellectual property is the concept of work-for-hire germane64.Cost Accounting StandardsIt is the ___________ that dictate the way in which a contractor must maintain its accounting system.65.Cost Accounting Standards (CAS) must be applied to awards:
a. without federal funding
b. received from any funding source
c. for federal contracts over $500,000
c. for all federal awards covered by 2 CFR 230 (OMB Circular A-122)c. for federal contracts over $500,00066.Cost of Living Allowance COLAgranted to employees based in a foreign city, where cost of living is higher than in Washington, D.C.67.Cost Principals for Educational InstitutesWho is the 2 CRF 220, OMB Circular A-21 for68.A cost reimbursement sub agreementRequires that the subrecipient use best efforts to complete the research

69.Cost sharing must be:
a. verifiable from records
b. included with other federal awards
c. paid from federal funds if it is a fellowship
d. donated third party contributionsa. verifiable from records70.cost sharing occurs when the sponsored program requires financial support for the project from the awarded institution as a condition of the award.What is involuntary committed (mandatory) cost sharing?71.Data Management Plan RequirementNo more than 2 pages and must describe how the proposal will conform to NSF policy on dissemination and sharing of research results.72.Data sharing plan/ Publish and ShareApplicant who are planning to share data may wish to describe briefly the expected scheduled for data sharing, the format of the final data set, the documentation to be provided, whether or not any analytic tools also will be provided and so on ...73.Debarment and suspension rulesWhich of the following is included in 2 CFR 215, OMB Circular A-110?74.Default and convenienceTwo critical termination clauses of the General Provisions of a federal contract75.Department of AgricultureWhich agencies is responsible for administering the Animal Welfare Act?76.Department of EnergyWhich of the following agencies does NOT fund health science research77.Director of Human ResourceWho should administer progressive discipline to an employee?78.the Director of the institution's animal careAs required an IACUC Committee must contain all but one of the following a. a Doctor or Veterinary Medicine, b. a practicing scientist experienced in research with animals, c. the Director of the institution's animal care facility, d. a person not affiliated with the institution79.Each calendar yearOMB Circular A-21, time and effort reporting must be submitted to the institution a MINIMUM of once

80.Each organization using animals in Public Health Service projects must provide written assurance of its compliance with:
a. regulations requiring full-time staff veterinarian
b. provisions for an organizational program for the care and use of animals
c. standard for accreditation with the American Association for Accreditation of Laboratory Animal Care
d. requirements for organizational training and instruction program in the human practices of animal care and used. requirements for organizational training and d. requirements for organizational training and instruction program in the human practices of animal care and use81.Efficient and effective operations and reliable financial reporting are the objectives of:
a. internal controls
b. research compliance
c. cost transfer processes
d. postaward administrationa. internal controls82.electronic funds transferThe federal government prefers to disburse funds under federal grants via83.enacted to assure that a fair portion of federal contracts are placed with small businesses.What is the Small Business Act?84.Equipment donated at fair market valueIs allowable as cost sharing85.Established fundamental national policy for the environment and established the council on environmental qualityWhat is the National Environmental Policy Act?86.Evaluation PlanIt is important to define carefully and exactly how success will be determined.

87.E-VerifyFAR 52.222-54, which requires that federal contractors or subcontractor verify the employment eligibility of all new hires on a contract through an electronic screening database.88.Every 3 yearsHow often do approved animal protocols need to be reviewed by the Institutional Animal Care and Use Committee (IACUC)89.Executive Branchbranch of the government is responsible for enforcing the laws of the land. The president, vice president, department heads (cabinet members), and heads of independent agencies carry out this mission.90.Executive Level II $181,500NIH Salary cap is at what percentage?91.Executive Level I, II, IIIWhat is the highest level of salary?92.Executive Orders 8248 and 11541Establishing the divisions of the Executive Office of the President and defining their functions and duties
Source and -Prescribing the duties of the Office of Management and Budget and the Domestic Council in the Executive Office of the President93.Expanded AuthoritiesDelegates to grantees authorization of one year, no cost extension94.Expanded Authority_____waives certain prior approval requirements by a federal sponsoring agency. It is used only for changes that are necessary for the completion of the project within its original scope and original total budget.95.FabricationMaking up data or results and recording or reporting them96.A facilities & administrative costs (indirect cots) rate is usually established based on:
a. prior actual costs
b. reimbursed costs
c. capital expenses
d. unaudited expensesa. prior actual costs

97.A facilities and administrative cost (indirect cost) may be a direct cost if:
a. it meets the definition of allocable
b. "unlike circumstances" are present
c. normally allowable on federal or federal flow-through awards
d. the award activities are like those generally charged as facilities and administrative costs (indirect costs)b. "unlike circumstances are present98.Faculty have share in the companyConflict of interest may exist when medical faculty members conduct drug clinical tests for a company if99.A faculty member has a 5-yar federal NIH grant which will terminate 8/31, with $14,000 remaining on 7/15 of the same year. A competing continuation was recommended for approval but not funded. Which of the following is the most appropriate advise for the research administrator to give to the member
a. buy as much equipment as possible before the grant year ends
b. request a second review of the continuation application for the NIH
c. transfer laboratory personnel salaries to the to use up the remaining funds
d. request a 1-year, no-cost extension of the grant while revised continuation is under preparationd. request a 1-year, no-cost extension of the grant while revised continuation is under preparation100.F&A is not allowed to be charged on the following?Participant support*, equipment, capital equipment, patient care, tuition, building renovations, rental costs for non-University owned space, scholarships/fellowships, Subawards in excess of $25,000. 
*NSF only

101.FalsificationManipulating research materials, equipment, or processes, or changing or omitting data or results such that the research is not accurately represented in the research record102.FARIn order for a contractor to be awarded a federal contract, he must comply with the provisions set forth by:103.FARThe overall guiding principle of __________ is to have an acquisition system that can satisfy customer's needs yet minimize administrative overhead without sacrificing integrity, fairness, openness and public policy objectives.104.A federal agency responsible for negotiating and approving facilities and administrative cost (indirect costs) rates for an educational on behalf of all other federal agencies in referred to as the:
a. lead agency
b. cognizant agency
c. sponsoring agency
d. governmental agencyb. cognizant agency105.Federal commonsWhat is an Internet grants management portal which serves the grantee organization community?106.Federal expanded authorities permit which of the following without additional sponsor approvals?
a. Rebudgeting
b. Change of the Institution
c. Renovation of laboratory space
d. Change of the principal investigatora. Rebudgeting107.Federal Financial Assistance Management Improvement Act 1999 Public Law 106-107The impetus to change the ways in which federal agencies accept grant applications and manage grant awards has

108.The federal government prefers to disburse funds under federal grants via:
a. letters of credit
b. reimbursement check
c. electronic funds transfer
d. advanced treasury checksc. electronic funds transfer109.Federal regulations governing the use of humans in researchAlways require full informed consent of the subject or the subject's guardian110.The first $25,000When a subaward is involved in a federal grant to a large university, on what portion of the subawardee's budget does the prime institution recover facilities and administrative cost(indirect cost)?111.FOA instructions always supersede these form instructions.If you have a funding opportunity announcement (FOA), which instructions do you go by... the research form or the FOA112.For copyrighted works which result from federally sponsored activities the federal government usually requires
a. disclosure of the copyright only
b. one copy of the official archives
c. a royalty-bearing , exclusive, and irrevocable license
d. a royalty-free, nonexclusive, and irrevocable licenseb. one copy of the official archives113.Formulation of the President's Budget;
Action by the Congress; Presentation (to Congress) and-Execution of enacted budget lawsWhat are the 3 main phases in the Federal Budget Process114.Freedom of Information Act (FOI)What act brought this on FFATA?

115.From any institution that receives more than $700,000 in federal fundingUnder which of the following conditions is a Certificate of Current Cost and Pricing required116.The Fulbright Program provides opportunities for
a. teaching abroad
b. service abroad
c. teaching n low income communities
d. construction of low income housinga. teaching abroad117.Goals/Objectives/SOW/ImplementationApplicant should explain the expected results and benefits of each objectives.118.House of Representativesa provision or report language included primarily at the request of a Member, Delegate, Resident Commissioner, or Senator providing, authorizing or recommending a specific amount of discretionary budget authority, credit authority, or other spending authority for a contract, loan, loan guarantee, grant, loan authority, or other expenditure with or to an entity, or targeted to a specific State, locality or Congressional district, other than through a statutory or administrative formula driven or competitive award process.119.How does an institution find their DUNS numberYou can contact your office of sponsored research or you can also log in to the eRA Commons.

120.How many days do recipients of federal grant funds have to submit final reports after completion of the project period?
a. 30 
b. 60
c. 90
d. 120c. 90121.How often do approved animal protocols need to be reviewed by the Institutional Animals Care and Use Committee (IACUC):
a. Annually
b. Semiannually
c. Every 2 years
d. Every 3 yearsd. Every 3 years122.How to do business internationallyThe Office of Commercial and Business Affairs (CBA) plays a major role in coordinating trade and investment matters to support U.S. firms doing business overseas. Our mission is to engage U.S. government resources to assist and promote U.S. business interests overseas, and to ensure that private sector business concerns are fully integrated into U.S. foreign and economic policy.123.iEdisonInteragency Extramural Invention Information Management System helps government grantees and contractors comply with a federal law, the Bayh-Dole Act regulations require that government funded inventions be reported to the federal agency who made the award

124.If a graduate student comes into a university sponsored research office charging that because of the federal Freedom on Information Act (FOIA) he has the right to obtain a copy of recently submitted proposal, the research administrator should
a. provide student with a complete copy of the proposal
b. provide student with a copy of the proposal with proprietary and salary information blacked out
c. advise student to apply to the federal agency to request a proposal 90 days after the proposal was submitted
d. tell the student to wait to apply to the federal agency until after the decision is made on the proposald. tell the student to wait to apply to the federal agency until after the decision is made on the proposal125.If an agency requires 20% cost sharing of the total project for a particular program and a proposal is requesting $200,000 from the agency, what is the additional amount that the institution must cost share?
a. $40,000
b. $50,000
c. $100,000
d. $220,000$50,000
$200000 / .8 = $250,000

$250,000-$200,000 = $50,000126.If an institution of higher education is subject to OMB Circular A-133, when must it have an independent audit?
a. Annually
b. Biennially
c. Triennially
d. At the discretion of its governing bodya. Annually127.If a principal investigator proposes to conduct research involving human subjects who will take a standardized educational test, but the test will not include any names or other identifying information, the proposal should be:
a. reviewed by the full Institutional Review Board
b. submitted for expedited review by the Institutional Review Board
c. submitted for review to the Office of Human Research Protection
d. treated under organization's policy as exempt from reviewb. submitted for expedited review by the Institutional Review Board

128.The impetus to change the ways in which federal agencies accept grant applications and manage grant awards has been mandated by:
a. e-Government strategies
b. new audit policies at the Office of Management & Budget
c. Office of Science & Technology Policy
d. the Federal Financial Assistance Management Improvement Act of 1999 (Public Law 106-107).d. the Federal Financial Assistance Management Improvement Act of 1999 (Public Law 106-107).129.indemnityOne may use what kind of clause to require that one party indemnify the other when certain expenses are incurred130.individual account in an approved accounting systemUpon receipt of awarded projects, educational institutions are required to establish131.Information is made available to the public by publication in the Federal Register, upon request given a description of the records desired and provides an opportunity to read and copy records at convenient locations.What is the Freedom of Information Act?132.In order for a foreign national student researcher to work on a federal grant in an American institution, it is necessary for the student to have:
a. a visa
b. United States citizenship
c. evidence of English proficiency
d. approval of student's embassya. a visa133.The Institutional Animal Care and Use Committee (IACUC) is required to inspect animal facilities a MINIMUM
a. one a month
b. twice a year
c. once a year
d. once every three yearsb. twice a year134.Institutional Biosafety CommitteeWhich of the following is mandated for the oversight of research involving recombinant DNA

135.Institutional National Research Service AwardsThe National Institutes of Health requires a written description of a program for providing instruction in the responsible conduct of research for136.The Institutional Official for a sponsored research projectThe individual authorized by the Board of Trustees to sign on behalf of the institution137.Institutions, InvestigatorsWho is covered by the COI regulation138.Institutions that have more than $25,000,000 in federal grants or contractsWhich of the following would be required to file a disclosure statement (DS-2) with the federal government?139.internal controlsEfficient and effective operations and reliable financial reporting are the objectives of140.International Traffic in Arms Regulations (ITAR) are controlled by the :
a. United Nations
b. U.S. Department of State
c. U.S. Department of Homeland Security
d. Bureau of Alcohol, Tobacco, and Firearmsb. U.S. Department of State141.In the credentials boxWhere do you put the ERA Login?142.In the event of cost overrun by a subcontractor, who would be held responsible by the funding sources?
a. Subcontractor only
b. Prime contractor only
c. Project director and subcontractor
d. Project directly and prime contractora. Subcontractor only

143.An investigator on an NIH grant has permission to rebudget $50,000 in supply monies into equipment. If the institution's facilities and administrative cost (indirect costs) rate (based on MTD) is 50%, how much money will be available for the equipment?
a. $25,000
b. $33,333
c. $50,000
d. $75,000d. $75,000

$50,000 X 1.50 = $75,000144.Involves a conflict of interestFaculty member is a major stockholder in a for profit company receiving a university contract145.Is a binding contract made between two parties, one of whom is the "Sponsor" or the company or individual sponsoring the clinical trial, while the other is the "Institution" or the organization or hospital receiving the sponsorship for conducting clinical trials.What is the Clinical Trial Agreement?146.Is intended to give credit where credit is due. Requires acknowledgement of Federal grant support when issuing statements, press releases, requests for proposals, bid solicitations, etc.What is the Stevens Amendment?147.is the grant of a property right to the inventor, issued by the Patent and Trademark Office. The term of a new patent is 20 years from the date on which the application was filedWhat is a patent?148.is to ensure that employers provide employees with an environment free from recognized hazards, such as exposure to toxic chemicals, excessive noise levels, mechanical dangers, heat or cold stress, or unsanitary conditions.What is the Occupational Safety & Health Act?149.Is usually riskier than a cost reimbursement contractWhich of the following best describes a fixed-price contract150.It is a public-private partnershipWhich of the following correctly describes FirstGov

151.It's required before an award at the proposal stage.If you don't have ERA Commons password, when is it required for an IRB?152.Judicial BranchCourts decide arguments about the meaning of laws and how they are applied. They also decide if laws violate the Constitution—this is known as judicial review, and it is how federal courts provide checks and balances on the legislative and executive branches.153."Just in time" initiatives postpone the submission of which of the following items until a decision to make an award is reached?
a. Full proposal
b. Budget justification
c. Certification and representations
d. Research background of principal investigatorc. certification and representations154.Land acquisitionIn a Construction Grant, which is allowable155.Law passed to protect certain species of marine mammals deemed as being in danger of extinctionWhat is the Marine Mammal Protection Act?156.Legislative BranchArticle I of the Constitution establishes the legislative or law making branch of government. It has a two-branch Congress—the Senate and the House of Representatives—and agencies that support Congress.157.Let SRO review the proposal then allow the PI to submitIf a federal agency requires a PI to submit online, what should be done158.Letter of supportA straight forward document stating that the institution is in support of the application to proceed and that it will host the proposed research should the application be successful.159.live, vertebrate animals onlyThe PHS policy governing the use and care of animals covers

160.Make sure budget/rates are accurate.If a PI submitted a proposal without going through the SRO office, what is our first concern?161.Mandates that a "Responsible Party" register and report results of certain "applicable clinical trials". Interventional studies of drugs, biologics, or devices that are subject to FDA regulations.What is the Food and Drug Administration Amendments Act (FDAAA)?162.Martial status of applicantUnder federal Equal Employment Opportunity provisions, a supervisor should NOT ask which of the following during an employment interview:163.Material Safety Data Sheet (MSDS) fileWhich of the following is essential to a Chemical Hygiene Plan?164.Material Transfer AgreementMTA165.Material transfer agreement (MTA)What is a contract that governs the transfer of tangible research materials between two organizations, when the recipient intends to use it for his or her own research purposes166.Material Transfer AgreementsRecommended so that disputes about use do not arise. __ are contractually binding upon the parties.167.A mechanism for procurement of a product or service with specific obligations for both sponsor and recipient. Designed to benefit the sponsor by achieving an expected outcome or product.What is a contract?168.Members of an Institutional Animal Care and Use Committee (IACUC) must be appointed
a. funding agency program officer
b. Office of Human Research Protection
c. responsible administrative official of the organization
d. research administrator responsible for the committeec. responsible administrative official of the organization

169.Member unaffiliated with the institutionAccording to federal regulations, which of the following must be included in an Institutional Review Board?170.minimum wages, maximum hours, child labor, convict labor and safe and sanitary working conditionsThe Walsh-Healey Public Contracts Act deals with issues on171.Modified total direct costIs a frequently used base for facilities and administrative cost (F&A) computation?172.modular budget is applicable only to R01, R03, R15, R21, and R34 applicationsIn an NIH Research Project Grant Program, which budget couldn't be over $25,000 in direct cost per year?173.The National Institutes of Health requires a written description of a program for providing instruction in the responsible conduct of research for:
a. program project grants
b. competing research project grants
c. noncompeting research project grants
d. Institutional National Research Service Awardsd. Institutional National Research Service Awards174.National Library of MedicineWhich of the following is located within the National Institutes of Health175.The National Science Foundation indicates decisions on the funding of grant proposals should normally takea
a. 2-4 months
b. 6-9 months
c. 10-12 months
d. 18-24 monthsb. 6-9 months176.Needs/Problem statementIt should be a clear and concise statement of the problem you want to solve with grant funds.

177.NIH: What are the main types of awardsResearch Grants (R series)
Career Development Awards (K series)
Research Training and Fellowships (T & F series)
Program Project/Center Grants (P series)178.NIH: What is Just-in-TimeRefers to the information that NIH will ask you to send after your application goes through initial peer review and is within the range of possible funding. NIH will need this information but does not require it with your application.179.Nondisclosure AgreementA Local Business wants to meet with a PI to discuss a product that they might agree to begin work on. What should be done?180.A Notice of Award typically includes which of the following?
a. Approval of facilities and administrative costs (Indirect Costs) rate
b. Award terms and conditions
c. Congressional approval
d. Guarantees for continuationb. Award terms and conditions181.Nuclear Regulatory CommissionStandards for handling radioactive materials are developed and monitored by the182.October 1The federal fiscal year begins:183.The Office and Grants and Contracts/Finance will monitor and draw cash on expenditures as appropriateThe university receives a grant from NIH that states the payment terms are DHHS Letter of Credit. This means:184.The office for Human Research Protection is administered by:
a. a private agency
b. a nonprofit foundation
c. an independent federal agency
d. a cabinet-level departmentd. a cabinet-level department

185.Office supplies, postage, administrative and clerical salaries, local telephone charges and general purpose equipmentThe following items should normally be treated as F&A cost except when the particular cost item can be justified as an exceptional need. What are some examples of exceptional need186.OMB Circular A-133The following establishes audit requirements and defines Federal responsibilities for implementing and monitoring these requirements for institutions of higher education and other nonprofit institutions receiving federal awards187.On an SF 424 Form, what does renewal, mean?requests additional funding for a period subsequent to that provided by a previous award and competes with all other applications.188.On an SF 424 Form, what does resubmission mean?has been previously submitted, but was not funded and is now being resubmitted.189.On an SF 424 Form, what does revision mean?proposes a change in 1) the Federal government's financial obligations or contingent liability from an existing organization, or 2) any other changes in the terms and conditions of the existing award, including requests for additional specific aims.190.Once each calendar year and is issued on a quarterly basisThe CFR is divided into 50 titles that represent broad areas subject to regulation and is published by the Federal executive agencies/departments. Each volume of the CFR is updated191.Payments to subjectsWhich of the following costs is allowable according to OMB Circular A-21?192.personnel salaries are increasedPrior approval from a federal agency is usually not needed when

193.The PHS policy governing the use and care of animals covers
a. live, vertebrate animals only
b. any animal use in research and training
c. animals involved in research only
d. animals that might otherwise be kept as pets onlya. live, vertebrate animals only194.PlagiarismThe appropriation of another person's ideas, processes, results, or words without giving appropriate credit195.A plan for expenditure of fundsWhich of the following must be included in every federal grant budget?196.Possible items could NIH request through Just-in-timeOther support Current and Pending, Certificate of IRB approval of proposed use of human subjects, Evidence of compliance with education in the protection of human subjects,Verification of IACUC approval of proposed use of live vertebrate animals197.Primary purpose of a federal cooperative agreementTo provide assistance with substantial involvement of the federal agency198.prior actual costA facilities and administrative cost (indirect cost) rate is usually established based on

199.Prior approval from a federal agency is usually NOT needed when:
a. the scope of work is changed
b. personnel salaries are increased
c. the principal investigator is changed
d. additional alterations costing more than $10,000 are madeb. personnel salaries are increased200.Prior intramural support should be addressed in the narrativeWhen applying for extramural support, in which of the following ways should the principal investigator address prior related intramural support?201.PrisonersWhich of the following populations has special protection as research participants under federal guidelines?202.Prisoners, pregnant women, mentally unstable, and minors.Who cannot participate in clinical trials203.Privacy Act of 1974When an agency contracts for the design, development, or operation of a system of records on individuals on behalf of the agency to accomplish an agency function, the agency must apply the requirements of which of the following acts204.Project travelWhich of the following is NOT included in the computation of an indirect cost rate205.Proposal Central or Foundation web site.What resource site do Private Foundations mostly submitted through?206.Proposal SolicitationRFP and RFA are examples of207.protection provided to the authors of "original works of authorship" including literary, dramatic, musical, artistic, and certain other intellectual works, both published and unpublishedWhat is a copyright?208.protects certain health information and requires naming a Privacy Official and written policy and procedures.What is the Health Insurance Portability and Accountability Act (HIPPA) Patient Privacy Rule?

209.protects people from discrimination based on sex in education programs or activities which receive Federal financial assistanceWhat is Title IX of the Education Amendments: Sex Discrimination?210.Protects the rights of employees and employers. Encourages collective bargaining. And curtails certain private sector labor and management practices, which can harm the general welfare of workers, businesses and the US economy.What is the National Labor Relations Act?211.Provides an entitlement of up to 12 weeks of job-protected, unpaid leave funding any 12-month period for the following reasons; birth and care of the employees child, or placement for adoption or foster care of a child with the employees; care of an immediate family member who has a serious health condition or care of the employees own serious health condition.What is the Family and Medical Leave Act?212.Provides labor standards for certain persons employed by federal contractors over $2500 furnishing services to federal agencies.What is the Service Contract Act?213.Provisions are intended to help secure the nation against bioterrorism acts.The act requires individuals and institutions to nor produce, acquire, retain (stockpile) or possess types and quantities of any biological materials including bona fide research.What is the US Patriot Act?214.provisions for an organizational program for the care and use of animalsEach organization using animals in Public Health Service sponsored projects must provide written assurance of its compliance with215.RebudgetingFederal expanded authorities permit which of the following without additional sponsored approval?

216.received from any funding sourceCost Accounting Standards (CAS) must be applied to awards217.The recipient of federal funds agrees that US flag air carriers will be used to transport personnel and property when costs are charged to these funds including any air transportation to from between or within a country other than the US when US flag air carriers are available.What is the Fly America Act?218.Recipients of federal grant funds must retain records for a MINIUMUM of:
a. 180 days after closeout
b. 18 month after the grant end date
c. 2 years after each grant budget year
d. 3 years from submission of final report of expenditured. 3 years from submission of final report of expenditure219.Refer employee to appropriate institution representativeWhich of the following is an appropriate response to sexual harassment reported by an employee in the work force?220.Regular dissemination of funding opportunitiesWhich of the following is most important in developing a program of available support with a grantee institution?221.The Regulation imposes a 6-year time limitationWhat is the time limitation for occurrences of research misconduct to be brought to the attention of an institution or the Department of Health and Human Services (HHS) (see § 93.105)222.remain with the institutionUnder federal grant conditions, the title to equipment must223.RentWhich would you charge against F&A?224.Rental or usage fees from equipment purchased with grant fundsWhich of the following is considered program income?

225.Request a one year, no cost extension of the grant while a revised continuation is under preparationA faculty member has a five year National Institutes of Health (NIH) grant which will terminate August 31, with $14,000 remaining on July 15 of the same year. A competing continuation was recommended for approval but not funded. Which of the following is the most appropriate advice for the research administrator to give to the faculty member?226.Required information on federal awards be made available to the public via single, searchable websiteWhat is the Federal Funding Accountability and Transparency Act (FFATA)?227.Requires employers to assure that employees hired are legally authorized to work in the US.What is Immigration Reform and Control Act (IRCA)?228.Requires the government to show 3 materials elements on all sole source contracts with a the current threshold applicable to all agencies is $700,000 for prime contracts awardedWhat is Truth in Negotiations Act?229.Research misconductWhat is defined as fabrication, falsification and plagiarism, and does not include honest error or differences of opinion230.responsible administrative official of the organizationMembers of an Institutional Animal Care and Use Committee (IACUC) must be appointed by the231.Responsible Conduct of Research (RCR).What process was created from America COMPETES act?232.Restricts the political activity of executive branch employees of the federal government, District of Columbia government, and some state and local employees who work in connection with federally funded programsWhat is the Hatch Act?233.Returned to the sponsoring agencyUpon completion of a federal grant, excess funds remaining in the account should be

234.RFPWhich of the following would serve the purpose of inviting proposals and specifying the general terms and conditions under which the relevant award can be made235.Roles and responsibilities of the Principal Investigator and other key personnelProper technical conduct of the research effort
Compliance with the terms and conditions of the sponsored agreement, Managing project funds within the approved budget
Timely completion and submission of required technical reports
Complying with all university and sponsor policies and procedures pertinent to the award236.Roles and responsibilities of the Sponsored Programs OfficeProviding accounting, Purchasing
Other administrative services to assist the principal investigators in: - managing the financial aspects of their projects
obtaining the necessary goods, services, and personnel to conduct the research effort, meeting sponsor needs for fiscal reports, Provides financial accounting to sponsors for the activity funded and is subject to federal audit.237.a royalty-free, nonexclusive, and irrevocable licenseFor copyrighted works which result from federally sponsored activities, the federal government usually requires238.Salaries and wagesWhich of the following is a base for facilities and administrative cost (indirect rate)?239.Salary or other payments for service, equity interests, intellectual property rights.Significant Financial Interest is defined by the regulation as anything of monetary value, including but not limited to:240.SF269The following is used to prepare quarterly, semi-annual, annual, or end reports241.SF270The following is used to request for an advance or reimbursement242.SF272The following is used to prepare a report of federal cash transactions243.Shelby AmendmentAccess to federally funded research data is required under the244.Should be closely followedWhich of the following is most appropriate use of federal agency guidelines for writing a proposal245.SponsorWhich of the following is responsible for clinical trial registration on ClinicalTrials.gov?

246.Standards for handling radioactive materials are developed and monitored by the:
a. Nuclear Regulatory Commission
b. Environmental Protection Agency
c. Centers for Disease Control and Prevention
d. Occupational Safety and Health Administrationa. Nuclear Regulatory Commission247.State and local governments are subject to which of the following OMB Circulars?
a. 2 CFR 220 (A-21)
b. A-102
c. 2 CFR 230 (A-122)
d. A-133b. A-102248.Subcontractor onlyIn the event of a cost overrun by a subcontractor, who would be held responsible by the funding source?249.Subcontractor's normal rateWhich of the following establishes the actual facilities and administrative cost (indirect cost) rate for a subcontract?250.Subcontract, Subgrant, or SubagreementA document written under the authority of, and consistent with the terms and conditions of an award, that transfers a portion of the research of substantive effort of the prime award to another institution or organization.251.System for Award Management (SAM)What is the name of the system for requiring submission and maintenance of representations and certifications252.Task Order Agreement TOAA legally binding document authorizing work and appropriating funds as a supplement to a basic contact.

253.teaching abroadThe Fulbright Program provides opportunities for254.Teaming AgreementAn agreement between two or more parties to participate in a research project or teaching activity255.Temporary rate subject to final negotiationWhich of the following best describes a provisional indirect cost rate256.They upload it to their submission application. Not on the SF 424 formIf a PI wants to request a reviewer to a proposal submission, where can they do this257.TitleIt should tell us in 25 words or less what you intend to research and should be relevant258.TravelWhich of the following expenses would be included in the distribution base of modified total direct costs?259.The travel costs do not provide any benefit to the federally sponsored projectA PI on a federally awarded grant wants to charge travel costs to a project for attendance at a conference that is unrelated to the project. Which of the following BEST explains why the PI cannot charge the travel costs to the project260.treated under organization's policy as exempt from reviewIf a principal investigator proposes to conduct research involving human subjects who will take a standardized educational test, but the test will not include any names or other identifying information, the proposal should be261.TrueUBMTA may not be usable for materials in projects supported by industry. True or False262.TrueA one-time no-cost extension up to 12 months is allowed as an expanded authority. True or False263.twice a yearThe Institutional Animal Care and Use Committee (IACUC) is required to inspect animal facilities a MINIMUM of

264.Under a federal contract, which of the following is a reason for termination for default?
a. Untimely performance
b. Budget revision
c. Cost overrun
d. Inadequate performance on another contracta. Untimely performance265.Under federal grant conditions, the title to equipment must
a. remain with the agency
b. remain with the institution
c. be vested with the institution only under $5,000
d. be vested in the institution with the agency's right to transfer to itself or another entityb. remain with the institution266.Under which of the following conditions is a Certificate of Current Cost and Pricing required?
a. For a federal contract over $1,000,000
b. For any federal subcontractor
c. From any institution that received more than $500,000 in federal funding
d. As a standard of certification submitted by institutions applying for federal grantsc. from an institution that received more than $500,000 in federal funding267.Uniform Biological Material Transfer Agreement (UBMTA)Makes one class of transfers routine
Standard terms developed in 1995 by NIH sponsored group
Provides standardized approach for certain transfers between academic institutions

268.Unilateral AwardAn award made by a sponsored to an organization without considering competitive proposals. They are most often made when unsolicited proposals receive favorable treatment.269.United States Department of Agriculture (USDA)is the U.S. federal executive department responsible for developing and executing federal government policy on farming, agriculture, forestry, and food. It aims to meet the needs of farmers and ranchers, promote agricultural trade and production, work to assure food safety, protect natural resources, foster rural communities and end hunger in the United States and abroad.270.United States Department of Homeland Securitya cabinet department of the United States federal government, created in response to the September 11 attacks, and with the primary responsibilities of protecting the United States and its territories (including protectorates) from and responding to terrorist attacks, man-made accidents, and natural disasters.271.United States Department of Veterans Affairsis a government-run military veteran benefit system with cabinet-level status. It is the United States government's second largest department, after the United States Department of Defense.272.unlike circumstances are presentA facilities and administrative cost (indirect cost) may be a direct cost if273.Untimely performanceUnder a federal contract, which of the following is a reason for termination for default?

274.Upon completion of a federal grant, excess funds remaining in the account should be :
a. returned to the sponsoring agency
b. transferred to another sponsored project
c. assigned to institution's general funds
d. included in proposal for an additional granta. returned to the sponsoring agency275.Upon receipt of awarded projects, educational institutions are required to establish?
a. credit card account for the investigator
b. combined accounts for easier investigator access
c. noninstitutional savings account for the investigators
d. individual accounts in an approved accounting systemd. individual accounts in an approved accounting system276.U.S. Department of Justice, under the False Claims ActWhich federal agency is responsible for prosecuting institutional violations of effort reporting277.U.S. Department of StateInternational Traffic in Arms Regulations (ITAR) are controlled by the278.Using the criteria contained in 2 CFR 220 (OMB Circular A-21), which of the following costs would most likely be allowable as a direct expenditure item on a federal grant?
a. Costs of preparing the grant proposal
b. Break refreshments at a project-sponsored workshop
c. Facility rental for a project staff holiday party
d. An amount specifically set aside for unanticipated expensesb. Break refreshments at a project-sponsored workshop279.Varies with funding sourceFederal regulations require that documentation of expenditures must be kept for how long?280.verifiable from recordsCost sharing must be

281.A vivariumWhat is an area, usually enclosed, for keeping and raising animals or plants for observation or research282.What are allowable costsAre costs that can be legitimately charged to a grant. An award refers to those funds that have been obligated by a funding agency for a specific project.283.What are Research Administrators?Advocate, Facilitator, Gatekeeper, Reviewer, Enforcer, Motivator, Resource Locator, Interpreter,Team Builder,Compliance Manager284.What are the roles and responsibilities of the InstitutionExpedite hiring of staff and faculty to enable work to proceed from the start of the award; Assist departments, schools, the Office of Research, and the Office of Research Accounting to facilitate administrative tasks; Meet the terms and conditions of the sponsored award in collaboration with the Investigators;-Provide timely and accurate monthly accounting reports to Investigators285.What determines if Financial Interest is SignificantFunds received for investigator and spouse/children meets both the following tests: 1) does not exceed $5000 in value as determined through reference to public prices or other reasonable measures of market value 2) does not represent more than a 5% ownership interest in any single entities.286.What is a Commercial And Government Entity Code (CAGE) and its purposeis a unique identifier assigned to suppliers to various government or defense agencies, as well as to government agencies themselves and also various organizations. It provide a standardized method of identifying a given facility at a specific location.287.What is a Data Universal Numbering System (DUNS Number)?is a system developed and regulated by Dun & Bradstreet that assigns a unique numeric identifier to a single business entity. That number is a nine-digit number issued to each business location in the D&B database having a unique, separate, and distinct operation for the purpose of identifying them.288.What is a grant?A type of financial assistance awarded for the conduct of research and no substantial programmatic involvement with the recipient during the performance of the activities.289.What is an Invitation For Bid (IFB)?the method used for the sealed bid process. A contract is then awarded to the low bidder whose bid conforms with all requirements of the invitation and will be advantageous to the government in terms of price, and price-related factors

290.What is a Request for Proposal (RFP)?occurs when the agency isn't certain about what it wants and is looking to you to develop a solution and cost estimate.291.What is a Request for Quote (RFQ)is often used to determine current market pricing, but is not a binding offer and can't be accepted by the government. A Standard Form 26, which requires the signatures of both the contractor and the contracting officer, would be required to make the offer binding.292.What is a Student Visa?Generally, a citizen of a foreign country who wishes to enter the United States must first obtain a visa, either a nonimmigrant visa for temporary stay, or an immigrant visa for permanent residence. You must have a student visa to study in the United States. Your course of study and the type of school you plan to attend determine whether you need an F-1 visa (academic) or an M-1 visa (vocational).293.What is Catalog of Federal Domestic Assistance (CFDA)?is a government-wide compendium of an online database listing all available federal programs.294.What is debarment?removes you as a contractor from eligibility for future government contracts for a fixed period of time.295.What is Drug Free Work ForceDOD contractors must maintain records regarding drug-free work force programs provided to their employees. Also establishes a program testing for the use of illegal drugs by employees.296.What is effort reportingThe percentage of total employment devoted to a particular project, activity, administrative task297.What is Equal Employment Opportunity?provide equal opportunity without regard to race, color, religion, sex, or nationality to persons employed or seeking employment298.What is Fair Labor Standards Act?Enacted to establish a minimum hourly wage, overtime pay and regulate child labor299.What is Health Resources and Services Administration (HRSA) and who do they fall underimproves access to healthcare for people who are uninsured, isolated, or medically vulnerable and under DHHS.

300.What is Lobbyingthe act of attempting to influence decisions made by officials in the government, most often legislators or members of regulatory agencies.301.What is Small Business Innovative Research (SBIR)?refers to the agency administered programs that are supported by ear-marked federal funds, making grants to small business entities302.What is Small Business Technology Transfer (STTR)?refers to the grant applications and/or programs for funding those small business that are teamed up with research institutions.303.What is suspension?temporarily debars a contractor for the duration of any agency investigation of the contractor or ensuing legal proceedings.304.What is the America COMPETES Act?America Creating Opportunities to Meaningfully Promote Excellence in Technology, Education and Science- focuses on increasing research investment
Strengthens STEM Research (science, technology, engineering and math) from elementary through grad school.305.What is the Buy America Act?Establish a general preference for domestic articles, materials/supplies to protect the American worker by saving and creating jobs.306.What is the Byrd Amendment?Institution must certify that no appropriated funds were or will be expended to pay any person for influencing or attempting to influence an officer or an employee of any agency, a member of Congress, an officer or employee of Congress in connection with a specific award.307.What is the Civil Rights Act?Bars recipients of federal funds from excluding persons because of race, sex, color, or national origin from participation in receiving benefits or otherwise subjecting them to discrimination under federally supported programs or activities. Law also interpreted to cover discrimination against those persons with limited English. Sex includes pregnancy, childbirth or related medical conditions.308.What is the Confidentiality of Patient Records?Enacted to protect persons with substance abuse problems who seek treatment.309.What is the Davis/Bacon ActRequires contractors to pay wages to laborers and mechanics at a rate of no less than a minimum wage specified in a wage determination made by the Secretary of Labor.

310.What is the Drug Free Workplace ActIt says you can't receive federal funding if you do not have a drug-free workplace policy in place311.What is the Endangered Species Act?species listed as endangered or threatened prohibits the unauthorized taking, possession, sale and transport of those species312.What is the Equal Pay Act?act prohibits employers and unions from paying different wages based on the employees sex313.What is the False Claims Act?Improper costing, product substitutions, failure to comply with contract specifications and filing false claims with government health care programs314.What is the percentage that all STTR budgets must matchAt least 40 percent of the STTR research project is to be conducted by the small business concern and at least 30 percent of the work is to be conducted by the single "partnering" research institution.315.What is the Ruth L. Kirschstein NSRA Award? Why is it importanttrain fellows and residents, and are used to promote the education of future researchers. She was a champion of research training and a strong advocate for the inclusion of underrepresented individuals in the scientific workforce316.What is the Solomon Act (Amendment)/ National Defense Authorization ActWhat United States federal law that allows the Secretary of Defense to deny federal grants (including research grants) to institutions of higher education if they prohibit or prevent ROTC or military recruitment on campus.317.What is use of name exceptionIt's an exception that agree that neither party will use directly or by implication names or trademarks of the other party in connection with any publicity, promotion or advertising without prior written approval.318.What is voluntary committed cost sharing?when the proposing institution volunteers and commits to bear a specific portion of the costs of the project when it is not required.319.What is voluntary uncommitted cost sharing?when the PI chooses to expend some unspecified amount of effort more than proposed towards the award. This is usually the case when the PI is not requesting salary from the award, and so is volunteering his/her effort.

320.When applying for extramural support, in which of the following ways should the PI address prior related support?
a. Prior intramural support should be ignored
b. Prior intramural support can be considered as an item of cost sharing in the budget narrative
c. Prior research related support should be considered unrelated in current grant request
d. Prior intramural support should be addressed in the narratived. Prior intramural support should be addressed in the narrative321.When a subaward is involved in a federal grant to a large university, on what portion of the subawardee's budget does the prime institution recover facilities and administrative costs (indirect costs)?
a. None of it
b. The first $25,000
c. The subawardee's modified total direct cost amount
d. The amount is excess of $25,000b. The first $25,000322.Whenever covered animals are involved in a protocolWhich of the following requires Institutional Animal Care and Use Committee (IACUC) review and approval governing the use of animals?323.When granted expanded authorities pre-award costs on a federal grant may be incurred by an institutional within
a MAXIMUM of how many days prior to the official start date:
a. 30 days
b. 45 days
c. 90 days
d. 120 daysc. 90 days

324.Which federal agency is responsible for prosecuting institutional violations of effort reporting?
a. U.S. Department of Justice, under the False Claims Act
b. Government Accountability Office, under the Code of Federal Regulations
c. Office of Management and Budget, under OMB Circular A-133 Audit Requirements
d. National Science Foundation Office of the Inspector General, under Congressional Oversight Authoritya. U.S. Dept of Justice, under the False Claims Act325.Which of the following agencies does NOT fund health science research?
a. U.S. Army
b. Department of Energy
c. National Institute of Aging
d. National Science Foundationd. National Science Foundation326.Which of the following agencies is responsible for administering the Animals Welfare Act?
a. Public Health Service
b. Department of Agriculture
c. Environmental Protection Agency
d. American Society for Prevention of Cruelty to Animalsb. Department of Agriculture327.Which of the following are two critical termination clauses of General Provisions of a federal contract:
a. Dispute and changes
b. Default and convenience
c. Default and stop work order
d. Stop work order and failure to confirmb. Default and convenience

328.Which of the following best describes 2 CFR 220 (OMB Circular A-21)?
a. Is applicable only to NSF and NIH
b. Allows federal agencies to places additional restrictions on individual items of costs
c. Deals with cost determination but does not identify the circumstances or dictate the participation in the financing of a project
d. Establishes principles for determining costs applicable to contracts, grants, and other agreements with both educational institutions and hospitalsc. Deals with cost determination but does not identify the circumstances or dictate the participation in the financing of a project329.Which of the following best describes federal regulations governing the use of humans in research?
a. Allow the researcher full discretion as to what to include in informed consent materials
b. Always require full informed consent on the subject or the subject's guardian
c. Allow the Institutional Review Board discretion in limited situations to approve protocols providing less than full informed consent
d. Waive full informed consent of the subject when the protocol is too complicated for an individual subject to understand the risksb. Always require full informed consent on the subject or the subject's guardian330.Which of the following delegates to grantee authorization of one year, no-cost extensions?
a. Expanded Authorities
b. Cost Accounting Standards
c. Public Law 106-107
d. Code of Federal Regulationsa. Expanded Authorities331.Which of the following establishes the actual facilities and administrative cost (indirect cost) rate for a subcontract?
a. Prime recipient's rate
b. Prime award agreement
c. Subcontractor's normal rate
d. Agreement between subcontractor and funding agencyc. Subcontractor's normal rate

332.Which of the following expenses would be include in the distribution base of modified total direct costs?
a. travel
b. equipment depreciation
c. sponsored programs office expenses
d. the portion of each subcontract in excess of $25,000b. equipment depreciation333.Which of the following information must be included in the notification by a federal officer to the contractor to terminate a contract for convenience?
a. Signature of program office
b. The effective date of the contract
c. A citation of the contract clause authorizing the termination
d. A specific statement defining the reason for the termination noticed. A specific statement defining the reason for the termination notice334.Which of the following involves a conflict of interest?
a. Faculty member owns and operates a business outside of university commitment
b. Faculty member consults with outside business in area of expertise
c. Faculty member supervises students employs them in university sponsored projects
d. Faculty member is a major stockholder in a for-profit company receiving a university contractd. Faculty member is a major stockholder in a for-profit company receiving a university contract335.Which of the following is a base for facilities and administrative costs (indirect costs)?
a. Subcontracts
b. Capital Equipment
c. Salaries and wages
d. Professional and outside servicesc. Salaries and wages336.Which of the following is a frequently used base for facilities and administrative costs (indirect cost) computations
a. Nonsalary costs
b. Capitalized equipment
c. Modified total direct cots
d. Total direct costs less pre-award costsc. Modified total direct cots

337.Which of the following is allowable as cost sharing?
a. Equipment donated at fair market value
b. Alcohol purchased for an allowable business dinner
c. A portion of the salary of the department head's secretary
d. Travel costs in excess of institutional per diema. Equipment donated at fair market value338.Which of the following is a primary purpose of a federal cooperative agreement?
a. To allow for flexible budgeting
b. To provide assistance with few restrictions
c. To enable solicitation by a Request of Proposal
d. To provide assistance with substantial involvement of federal agencyd. To provide assistance with substantial involvement of federal agency339.Which of the following is essential to a Clinical Hygiene Plan?
a. Material Safety Data Sheet (MSDS) file
b. Monthly fire and safety drills
c. Public information program
d. Federal Food & Drug Administration inspectiona. Material Safety Data Sheet (MSDS) file340.Which of the following is included in 2 CFR 215 (OMB Circular A-110)?
a. Audit requirements
b. Debarment and suspension rules
c. Federal contact requirements
d. Cost principles for nonprofitsb. Debarment and suspension rules341.Which of the following is located within the National Institutes of Health?
a. National Library of Medicine
b. Centers for Disease Control and Prevention
c. Food and Drug Administration
d. National Institute for Occupational Safety and Healtha. National Library of Medicine

342.Which of the following is mandated for the oversight of research involving recombinant DNA?
a. rDNA Committee
b. Biosafety Ethics Committee
c. Institutional Biosafety Committee
d. Institutional Biohazard Committeec. Institutional Biosafety Committee343.Which of the following is most important in developing a program of available support within a grantee institution?
a. Hiring of information specialist
b. Regular dissemination of funding opportunities
c. Development of subject-related database
d. Establishment of potential investigator fileb. Regular dissemination of funding opportunities344.Which of the following is responsible for clinical trail registration of Clinical Trials.gov?
a. Sponsor
b. Institution
c. Sponsored research office
d. Institutional Review Board (IRB)a. Sponsor345.Which of the following populations has special protection as research participates under federal guidelines?
a. Elderly
b. Prisoners
c. College Students
d. Persons diagnosed as HIV positiveb. Prisoners346.Which of the following requires Institutional Animal Care and Use Committee (IACUC) review and approval governing the use of animals?
a. When any animal is used
b. Only when laboratory animals are used in instruction
c. Whenever covered animals are involved in a protocol
d. Only if a protocol involve sacrificing animalsc. Whenever covered animals are involved in a protocol347.Which of the following sources in NOT commonly used for FEDERAL funding opportunites:
a. The Federal Register
b. The Foundation Directory
c. Commerce Business Daily
d. The Catalog of Federal Domestic Assistanceb. The Foundation Directory

Take courses from CCRPS and learn more on how to become a clinical research professional.

Here are some courses you might consider:

• Clinical Research Coordinator Certification - Ideal for those looking to coordinate clinical trial activities.

• Pharmacovigilance Certification - Focuses on drug safety and adverse effects management.

• CRA Certification - Prepares you for the role of Clinical Research Associate.

• ICH-GCP Certification - Essential for professionals needing to understand Good Clinical Practice guidelines.

• Clinical Trials Assistant Training - Provides foundational knowledge for those starting in clinical trials.

• Advanced Clinical Research Project Manager Certification - For experienced professionals aiming for project management roles.

• Advanced Principal Investigator Physician Certification - Tailored for physicians leading clinical trials.

• Medical Monitor Certification - Designed for those overseeing the medical aspects of clinical trials.

Discover more from Clinical Research Training | Certified Clinical Research Professionals Course

Among the most important aspects of study is observation. Overseeing the advancement of any stage, measure, process, and procedure in real time is essential to the accurate conclusion of any clinical trial undertaking. Normal monitoring actions are needed to guarantee caliber, efficiency, compliance within predefined and regulations fundamentals. In addition, it guarantees comprehensiveness, and precision within clinical investigation. Such actions also ensure that the trial isn't just conducted in compliance with Standard Operating Procedures (SOPs). They must also function to validate it is correctly reported and recorded. Consider enrolling in the Clinical Research Coordinator course or the CRA training provided by CCRPS.

There demands something vital as a part in the execution of trials. And this thing is known as trial development reports.

Such a report ought to be carefully prepared and it must summarize the means that a study is done. It also ought to point out recruiting progress and procedures; should emphasize and clarify adjustments to the analysis, and ought to point security issues. If you're involved in such reporting or need an in-depth understanding of the procedures, the Advanced Clinical Research Project Manager Certification might be of interest.

Aside from the ethics committee, researchers could also need to present yearly improvement reports of an investigation (such as any applicable alterations or dangers) to spouses, encouraging associations, and/or organizations, along with other interested parties if needed. To understand more about these requirements and get certified, the ICH-GCP course is an excellent resource.

If you're thinking about getting important skills on GCP or you also would like to upgrade your own know-how, subscribe to our comprehensive Good Clinical Practice class here.

In summary, tracking and reporting processes is an incredibly significant function in clinical trials. The right conduct of these procedures ensure compliance with legislation, regulations, and predetermined conditions. In addition, they make certain that the study doesn't pose any dangers to wellbeing. Progress reports, subsequently, empower practitioners, specialists, researchers, ethics committees, as well as others involved to keep a tab on the trial and its own advancement. Clinical professionals need to signal any alterations or risks to react to them timely, correctly, and efficiently. For further training, consider the Pharmacovigilance Certification to deepen your knowledge in monitoring drug safety.

The objective of progress reports would be to accumulate and outline upgrades, key facets, along with summaries of a continuing trial. It's very crucial to be aware that progress reports must be filed to institutional evaluation board/independent integrity questionnaire (IRB/IEC), following a trial that has obtained positive opinion.

One other important issue to mention is there are many different forms and when it comes to submitting progress reports that researchers must take into consideration before proceeding.

Precisely, these kinds are:

• Printing name and date of entry ought to be composed also. A digital copy is also needed to be delivered to the interested websites and committees inside a 30-day interval following the reporting procedure was completed.

• The period of time whereby an advance report ought to be filed is at least one time in a year. Nevertheless, based upon the situation as well as the RECs' needs, these reports might be passed in more often, although the analysis is still going and till its official conclusion date.

Take courses from CCRPS and learn more on how to become a clinical research professional. For detailed guidance on submission requirements and processes, the Medical Monitor Certification and Advanced Principal Investigator Physician Certification can provide extensive knowledge.

Discover more from Clinical Trials Assistant Training | Clinical Research Training | Certified Clinical Research Professionals Course to further your career in clinical research management.

Skills Alliance Clinical Research Associate - CRA Course

Clinical Research Associate Job available - CRA Course

$113,368 per year

Advanced Clinical Clinical Research Associate

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$107,750 per year

Syneos Health Commercial Solutions Clinical Research Associate

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$98,894 per year

Piper Companies Clinical Research Associate

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$101,820 per year

Novella Clinical Clinical Research Associate

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$97,659 per year

Covance Clinical Research Associate

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$96,667 per year

Premier Research Clinical Research Associate

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$95,178 per year

Syneos Health Clinical Clinical Research Associate

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$93,469 per year

PRA Health Sciences Clinical Research Associate

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$76,150 per year

Novo Nordisk, Inc. Clinical Research Associate

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$95,242 per year

PPD Clinical Research Associate

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$91,293 per year

IQVIA Clinical Research Associate - CRA Course

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$89,615 per year

Cyberonics Clinical Research Associate

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$87,000 per year

AbbVie Clinical Research Associate - CRA Course

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$81,391 per year

ICON plc Clinical Research Associate - CRA Course

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$79,110 per year

PAREXEL Clinical Research Associate - CRA Course

Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).

Clinical Research Associate Job available

$81,281 per year

QuintilesIMS Clinical Research Associate - CRA Course

11 salaries

Clinical Research Associate Job available

$72,749 per year

MD Anderson Cancer Center Clinical Research Associate - CRA Course

7 salaries

Clinical Research Associate Job available

$71,410 per year

Chiltern International Clinical Research Associate - CRA Course

5 salaries

$87,722 per year

Pharmanet Clinical Research Associate - CRA Course

5 salaries

$72,488 per year

Roche Clinical Research Associate - CRA Course

5 salaries

Clinical Research Associate Job available

$71,586 per year

University of Florida Clinical Research Associate - CRA Course

11 salaries

Clinical Research Associate Job available

$69,492 per year

Department of Veterans Affairs Clinical Research Associate - CRA Course

6 salaries

Clinical Research Associate Job available

$66,274 per year

Abbott Laboratories Clinical Research Associate - CRA Course

6 salaries

Clinical Research Associate Job available

$66,095 per year

University of Utah Clinical Research Associate - CRA Course

19 salaries

Clinical Research Associate Job available

$66,775 per year

University of Minnesota Clinical Research Associate - CRA Course

8 salaries

Clinical Research Associate Job available

$64,600 per year

University of Connecticut Health Center Clinical Research Associate - CRA Course

8 salaries

Clinical Research Associate Job available

$58,321 per year

St. Jude Children's Research Hospital Clinical Research Associate - CRA Course

6 salaries

Clinical Research Associate Job available

$56,315 per year

Northwestern University Clinical Research Associate - CRA Course

6 salaries

Clinical Research Associate Job available

$54,342 per year

Duke Clinical Research Institute Clinical Research Associate - CRA Course

5 salaries

$73,447 per year

Emory University Clinical Research Associate - CRA Course

5 salaries

Clinical Research Associate Job available - CRA Course

$50,778 per year

Medpace Clinical Research Associate

6 salaries

Clinical Research Associate Job available

$50,958 per year

University of South Florida Clinical Research Associate

20 salaries

Clinical Research Associate Job available

$50,810 per year

The University of Iowa Clinical Research Associate

26 salaries

Clinical Research Associate Job available

$43,547 per year

Yale University Clinical Research Associate

5 salaries

Clinical Research Associate Job available

$40,378 per year

University of Maryland, Baltimore Clinical Research Associate

7 salaries

Clinical Research Associate Job available

$39,818 per year

University of North Carolina at Chapel Hill Clinical Research Associate

7 salaries

Clinical Research Associate Job available

$38,402 per year

University of North Carolina at Greensboro Clinical Research Associate

5 salaries

Clinical Research Associate Job available

$38,475 per year

Virginia Commonwealth University Clinical Research Associate

19 salaries

Clinical Research Associate Job available

$36,453 per year

University of North Carolina Clinical Research Associate

15 salaries

$36,955 per year

University of Pittsburgh Clinical Research Associate

13 salaries

Clinical Research Associate Job available

$33,878 per year

SUNY Downstate Medical Center Clinical Research Associate

9 salaries

Clinical Research Associate Job available

$33,343 per year

Washington University in St. Louis Clinical Research Associate

18 salaries

Clinical Research Associate Job available

$15.75 per hour

UC San Diego Clinical Research Associate

19 salaries

Clinical Research Associate Job available

$4,353 per month

University of California - San Francisco Clinical Research Associate

6 salaries

Clinical Research Associate Job available

$100 per day

Real Staffing Clinical Research Associate

15 salaries

Clinical Research Associate Job available

$31.95 per hour

University of Nebraska Medical Center Clinical Research Associate

12 salaries

Clinical Research Associate Job available

$15.81 per hour

Texas Tech University Health Sciences Center Clinical Research Associate

6 salaries

Clinical Research Associate Job available

$3,609 per month

Aerotek Clinical Research Associate

8 salaries

$47.68 per hour

Randstad Clinical Research Associate

35 salaries

$45.90 per hour

Ohio State University Clinical Research Associate

124 salaries

Clinical Research Associate Job available

$14.49 per hour

University of Kentucky Clinical Research Associate

59 salaries

Clinical Research Associate Job available

$21.63 per hour

Biotech Partners Clinical Research Associate

12 salaries

Clinical Research Associate Job available

$111,431 per year

DOCS Global Clinical Research Associate

14 salaries

Clinical Research Associate Job available

$90,856 per year

CyberCoders Clinical Research Associate

28 salaries

$88,409 per year

Zp group Clinical Research Associate

18 salaries

$98,008 per year

CIG Clinical Research Associate

109 salaries

$116,784 per year

CorTech, LLC Clinical Research Associate

40 salaries

$38.91 per hour

Skills Alliance (Recruiting Company) Clinical Research Associate

12 salaries

$71.01 per hour

InfoStaff Clinical Research Associate

52 salaries

$109,699 per year

Stony Brook University Clinical Research Associate

5 salaries

Clinical Research Associate Job available

$39,254 per year

Brio Resource Group Clinical Research Associate

46 salaries

Clinical Research Associate Job available

$129,987 per year

Planet Pharma Clinical Research Associate

7 salaries

Clinical Research Associate Job available

$117,458 per year

biorasi LLC Clinical Research Associate

18 salaries

$63,702 per year

Intermountain Home Care Clinical Research Associate

11 salaries

$15.55 per hour

Piper Clinical Solutions Clinical Research Associate

16 salaries

$64,853 per year

Personify Clinical Research Associate

36 salaries

$99,373 per year

Segal Trials Clinical Research Associate

24 salaries

$2,195 per month

Bertram & Associates Clinical Research Associate

7 salaries

$116,417 per year

Lodestar Executive Search Clinical Research Associate

7 salaries

$116,417 per year

PSU Personnel Services Unlimited, Inc. Clinical Research Associate

6 salaries

$104,485 per year

The Hastings Group Clinical Research Associate

7 salaries

$116,417 per year

Ploeger Recruiting Services Clinical Research Associate

6 salaries

$104,485 per year

Phillips Staffing Solutions Clinical Research Associate

6 salaries

$104,485 per year

PMG Employment Consultants Clinical Research Associate

7 salaries

$116,417 per year

Bio-Partners Clinical Research Associate

7 salaries

$116,417 per year

Hire Horizons Clinical Research Associate

6 salaries

$104,485 per year

SearchStars Clinical Research Associate

6 salaries

$104,485 per year

Fowler Placement Services, Inc. Clinical Research Associate

6 salaries

$104,485 per year

Plastic Executive Recruiters Clinical Research Associate

6 salaries

$104,485 per year

EPM Scientific Clinical Research Associate

13 salaries

Clinical Research Associate Job available

$98,268 per year

Barrington James Clinical Research Associate

12 salaries

Clinical Research Associate Job available

$124,820 per year

MedExec International Clinical Research Associate

6 salaries

$104,485 per year

Tri-Force Clinical Research Associate

7 salaries

$116,417 per year

Professional Recruiting Partners, LLC Clinical Research Associate

7 salaries

$116,417 per year

Career Brokers, Inc. Clinical Research Associate

6 salaries

$104,485 per year

Helffrich International Clinical Research Associate

6 salaries

$104,485 per year

Tailored Management Clinical Research Associate

10 salaries

$79,138 per year

MJ Recruiters, LLC Clinical Research Associate

6 salaries

$104,485 per year

Meet Recruitment Clinical Research Associate

12 salaries

$102,820 per year

University of Virginia Clinical Research Associate

16 salaries

Clinical Research Associate Job available

$44,455 per year

Medical University of South Carolina Clinical Research Associate

20 salaries

Clinical Research Associate Job available

$32,233 per year

Oregon Health Sciences University Clinical Research Associate

17 salaries

Clinical Research Associate Job available

$43,176 per year

AutoPro Technical Recruiting Clinical Research Associate

6 salaries

$104,485 per year

MMS Group Clinical Research Associate

6 salaries

$104,485 per year

ONESource Technical Clinical Research Associate

6 salaries

$104,485 per year

Technology Recruiting Solutions, Inc. Clinical Research Associate

6 salaries

$104,485 per year

BRUNEL CANADA Clinical Research Associate

20 salaries

$83,573 per year

Affinity Executive Search Clinical Research Associate

20 salaries

$111,284 per year

PPD Development, L.P. Clinical Research Associate

11 salaries

$92,737 per year

HireNetworks Clinical Research Associate

12 salaries

Clinical Research Associate Job available

$94,478 per year

CMC Limited Clinical Research Associate

13 salaries

$111,719 per year

CMD And Associates Clinical Research Associate

17 salaries

$97,982 per year

fulltimeGiGS Clinical Research Associate

10 salaries

$120,496 per year

Cameron Craig Group Clinical Research Associate

17 salaries

$88,715 per year

Prevalent Group Clinical Research Associate

17 salaries

$95,522 per year

True North Consultants Clinical Research Associate

6 salaries

$104,485 per year

Financially Stable Pharmaceutical Clinical Research Associate

8 salaries

$112,472 per year

JDP Search Group Clinical Research Associate

16 salaries

$99,326 per year

PeopleStaff Clinical Research Associate

15 salaries

$84,270 per year

Clinical Management Consultants Clinical Research Associate

9 salaries

Clinical Research Associate Job available

$115,881 per year

JOHNLEONARD Clinical Research Associate

8 salaries

Clinical Research Associate Job available

$61,509 per year

Rangam Consultants Inc. Clinical Research Associate

5 salaries

Clinical Research Associate Job available

$72,617 per year

Keshav Consulting Solutions Clinical Research Associate

13 salaries

$60,670 per year

Onboard.jobs Clinical Research Associate

15 salaries

$94,156 per year

Cor-Tech LLC Clinical Research Associate

15 salaries

$42.97 per hour

Klinexa Inc. Clinical Research Associate

8 salaries

$25.00 per hour

Systematic business consulting Clinical Research Associate

13 salaries

$88,299 per year

University of Miami Miller School of Med Clinical Research Associate

8 salaries

$74,809 per year

Global Channel Management, Inc. Clinical Research Associate

12 salaries

$41.26 per hour

Productive Data Solutions, INC. Clinical Research Associate

8 salaries

Clinical Research Associate Job available

$27.00 per hour

Selective Staffing Solutions Clinical Research Associate

8 salaries

Clinical Research Associate Job available

$19.49 per hour

Atlanta Center for Medical Research Clinical Research Associate

5 salaries

$33,642 per year

DOCS Clinical Research Associate

10 salaries

$78.22 per hour

Impact Business Group Clinical Research Associate

12 salaries

$54.45 per hour

CPS Recruitment Clinical Research Associate

7 salaries

$28.46 per hour

SCOPE International USA, Inc. Clinical Research Associate

11 salaries

$80,886 per year

Interview with Center for Advanced Obstetrical Care and Research Clinical Research Associate

8 salaries

$17.00 per hour

Inflamax Research Inc. Clinical Research Associate

6 salaries

$2,900 per month

Priority Sales Recruiting Clinical Research Associate

11 salaries

$108,226 per year

University of Texas Medical Branch Clinical Research Associate

5 salaries

Clinical Research Associate Job available

$16.50 per hour

Eastern Virginia Medical School Clinical Research Associate

10 salaries

Clinical Research Associate Job available

$82,730 per year

Computech Corporation Clinical Research Associate

7 salaries

$45.00 per hour

Details on application Clinical Research Associate

9 salaries

$205,058 per year

BK Rich Associates Clinical Research Associate

6 salaries

$90,000 per year

Central Florida Careers Clinical Research Associate

9 salaries

$16.93 per hour

Chipton Ross Clinical Research Associate

10 salaries

$34.37 per hour

AppleOne Clinical Research Associate

10 salaries

$75,534 per year

Sabio Systems Clinical Research Associate

9 salaries

$19.90 per hour

Blair Search Clinical Research Associate

7 salaries

$116,417 per year

Sponsor Pharmaceutical company Clinical Research Associate

9 salaries

$110,000 per year

Helix Biomedics LLC Clinical Research Associate

6 salaries

$12.00 per hour

Ability Professional Network Clinical Research Associate

9 salaries

$95,663 per year

Leading CRO Company!! Clinical Research Associate

5 salaries

$99,504 per year

The Pursell Group Clinical Research Associate

7 salaries

$116,417 per year

PeaceHealth Clinical Research Associate

9 salaries

$35.36 per hour

new england physician recruitment center-boston Clinical Research Associate

9 salaries

$180,000 per year

MBA IT Consulting Services, Inc. Clinical Research Associate

7 salaries

$116,417 per year

Food Management Search Clinical Research Associate

7 salaries

$116,417 per year

Pharmaceutical Organization Clinical Research Associate

8 salaries

$246,884 per year

Texas Tech University Health Sciences Center of El Paso Clinical Research Associate

5 salaries

Clinical Research Associate Job available

$15.64 per hour

University of Wisconsin–Madison Clinical Research Associate

8 salaries

Clinical Research Associate Job available

$40,257 per year

Careers 2005 Clinical Research Associate

6 salaries

$104,485 per year

Taylee Staffing Clinical Research Associate

8 salaries

$102,227 per year

Rayco Technical Solutions, LLC Clinical Research Associate

6 salaries

$104,485 per year

Nishom Pharma Corp Clinical Research Associate

6 salaries

$70,000 per year

The Research Foundation for The State University of New York at Stony Brook Clinical Research Associate

5 salaries

$57,250 per year

Real Life Sciences Clinical Research Associate

7 salaries

$117,035 per year

Inflamax Research Clinical Research Associate

6 salaries

$2,900 per month

Aptude Inc. Clinical Research Associate

7 salaries

$20.00 per hour

Virginia Commonwealth University Clinical Research Associate

8 salaries

Clinical Research Associate Job available

$36,729 per year

Scientific Search Clinical Research Associate

7 salaries

Clinical Research Associate Job available

$85,322 per year

ER Squared, Inc. Clinical Research Associate

6 salaries

$50,000 per year

Valesta Clinical Research Solutions Clinical Research Associate

7 salaries

$65,000 per year

On-Board Services Clinical Research Associate

5 salaries

$38.67 per hour

Military4Hire Clinical Research Associate

6 salaries

$104,485 per year

SSC Clinical Research Associate

8 salaries

$115,000 per year

Enterprise Search Associates Clinical Research Associate

6 salaries

$104,485 per year

The Fountain Group Clinical Research Associate

8 salaries

$135,000 per year

VetPharm, Inc. Clinical Research Associate

8 salaries

$47,500 per year

Pioneer Data Systems, Inc. Clinical Research Associate

7 salaries

Clinical Research Associate Job available

$50.00 per hour

The University of Michigan Clinical Research Associate

6 salaries

Clinical Research Associate Job available

$60,183 per year

North Peak Recruiting Clinical Research Associate

6 salaries

$104,485 per year

MedicusTek USA, Inc Clinical Research Associate

7 salaries

$42,000 per year

Genesis Global Management Corporation Clinical Research Associate

7 salaries

$105,971 per year

Quality Clincial Research Clinical Research Associate

5 salaries

$28,802 per year

The Job Jobber Clinical Research Associate

7 salaries

$88,043 per year

IMARC Research, Inc. Clinical Research Associate

5 salaries

$15.52 per hour

PHAIDON INTERNATIONAL Clinical Research Associate

6 salaries

$109,198 per year

Experis Clinical Research Associate

7 salaries

$38.63 per hour

Sunrise Systems Clinical Research Associate

7 salaries

$29.69 per hour

Small Niche CRO! Clinical Research Associate

6 salaries

$88,364 per year

University of Toledo Clinical Research Associate

5 salaries

$66,079 per year

Resource Employment Solutions Clinical Research Associate

6 salaries

$24.04 per hour

RELODE Clinical Research Associate

6 salaries

$5,000 per month

Painter & Associates Personnel Clinical Research Associate

6 salaries

$104,485 per year

Provident Research Inc Clinical Research Associate

6 salaries

$113,374 per year

RBW Consulting Solutions Ltd Clinical Research Associate

5 salaries

$109,280 per year

ParkPower Corporation Clinical Research Associate

5 salaries

$120,496 per year

Acara Solutions Clinical Research Associate

5 salaries

$19.80 per hour

Essentia Health Clinical Research Associate

5 salaries

Clinical Research Associate Job available

$16.73 per hour

New York State Psychiatry Institute Clinical Research Associate

5 salaries

Clinical Research Associate Job available

$45,068 per year

BRIDGEWAY COMMERCE GROUP Clinical Research Associate

5 salaries

$120,496 per year

NuWest Group Clinical Research Associate

5 salaries

$16.43 per hour

Pharmaceutical Clients Clinical Research Associate

5 salaries

$30.00 per hour

Byrnes and Rupkey, Inc. Clinical Research Associate

5 salaries

$120,496 per year

Cap & Sol Clinical Research Associate

5 salaries

$50.00 per hour

RCTS, Inc Clinical Research Associate

5 salaries

$13.15 per hour

All US Jobs Clinical Research Associate

5 salaries

$120,000 per year

The DAVIS Companies Clinical Research Associate

5 salaries

$25.00 per hour

JGB BioPharma Consulting Inc. Clinical Research Associate

5 salaries

Clinical Research Associate Job available

$112,945 per year

Advanced Technology Solutions Clinical Research Associate

5 salaries

Clinical Research Associate Job available

$43.55 per hour

Worldwide Clinical Trials Holdings, Inc. Clinical Research Associate

5 salaries

$109,545 per year

Private Practice Leadership, LLC Clinical Research Associate

5 salaries

$15.71 per hour

Team1Medical Clinical Research Associate

5 salaries

$33,786 per year

ZEISS Group Clinical Research Associate

5 salaries

$48.00 per hour

Worldwide Placement Limited Clinical Research Associate

5 salaries

$90,000 per year

Pharmaceutical Research Associates, Inc. Clinical Research Associate

5 salaries

$76,530 per year

Healthcare Recruiters International Clinical Research Associate

5 salaries

$62,430 per year

Bridgeway Professionals Clinical Research Associate

5 salaries

$120,496 per year

i-Pharm Consulting Clinical Research Associate

5 salaries

Clinical Research Associate Job available

$94,767 per year

Collaborative Clinical Research Associate

5 salaries

$39.65 per hour

The Veritas Healthcare Solutions LLC Clinical Research Associate

5 salaries

$78,850 per year

Louis Stokes Cleveland VA Medical Center Clinical Research Associate

5 salaries

$43,399 per year

Piper Enterprise Solutions Clinical Research Associate

5 salaries

$111,929 per year

Groupware Solutions Clinical Research Associate - CRA Course

5 salaries

$30.00 per hour

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