The First Step to Clinical Research Certificate Program

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CCRP CRRA Certified Clinical Researcher Associate

This program requires only a medical sciences education background such as FMGs, BSNs, and Bachelors graduates. Clinical Research Associate Training Course is a 110 module course led by Senior CRA and Physician of 25 Years, Dr.Kamal. This course provides the training, experience, interviewing, letter of references, and connections you need to get a job supervising clinical research efforts. We offer clinical research associate training and placement for nurses, science bachelor graduates, and international medical graduates.

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SCDM CCDM Certified Clinical Data Manager

Eligibility Requirements

APPLICANTS FOR THE CERTIFIED CLINICAL DATA MANAGER (CCDM™) PROGRAM MUST MEET ONE OF THE FOLLOWING CRITERIA

• Bachelor’s degree or higher and minimum two years full-time CDM experience

• Associate’s degree and minimum three years full-time CDM experience

• Four or more years full-time CDM experience

• Part-time work experience equal to or surpassing full-time equivalent in criteria above

ACRP CCRA Certified Clinical Research Associate

The CCRA® eligibility criteria define the minimum experience required before a CRA can apply for the program. It is important to compare the CRA eligibility criteria with your career and educational experiences to self-determine your eligibility before submitting an application and payment. All applications must undergo a formal review process to determine an applicant’s eligibility to sit for the exam.

CRA Certification Eligibility Requirements

In order to be deemed eligible to take the CCRA® exam, applicants for the CCRA® credential must be able to provide evidence through a job description, detailed CV, or other documentation that they:

• Work independently of the investigative staff conducting the research at the site or institution. This means they do not report to the PI or site manager and that they do not have the ability to change or manipulate data, and;

• Work on behalf of the sponsor. This means that they are contracted by the “sponsor” to perform an independent monitoring function. The “sponsor” can be a pharmaceutical or device company, a granting agency, a university department, a physician, etc., and;

• Perform all of the CCRA® essential duties as detailed below for a required minimum number of hours. Hours performing the CRA essential duties can include hoursdocumented up to the date of the exam and/or through previous employment. The required number of hours is dependent upon one’s educational background.

The CRA Certification Handbook has complete information on eligibility requirements.

ACRP CCRC Certified Clinical Research Coordinator

CRC Certification Eligibility Requirements

In order to be deemed Eligible to take the CCRC® exam, applicants for the CCRC® credential must be able to provide evidence through a job description, detailed CV or other documentation that they:

• Perform all of the CRC essential duties as detailed below for a required minimum number of hours.

• Hours performing the CRC essential duties can include hours documented up to the date of the exam and/or through previous employment. The required number of hours is dependent upon one’s educational background.

SoCRA CCRP Certified Clinical Research Professional

The applicant must be working with Good Clinical Practice (GCP) guidelines under IRB/IEC/REB-approved (or specifically exempted) protocols.

The applicant must meet one of the following Eligibility Criteria noted below.   Please note that most candidates will be eligible under Category 1. 

For purposes of eligibility, please view SOCRA's definition of a Clinical Research Professional.

If you have a question about Candidate Eligibility please email SOCRA at certification@socra.org

Category 1

Applicant must have (and be able to document) ALL of the following qualifications:

• Have two years of experience as a full-time Clinical Research Professional (or have 3,500 hours part-time) during the last five years

Please note:  If you have completed two (2) years of full-time employment as a clinical research professional in the past five years, you will NOT need to provide supporting documentation for your educational experience.

Category 2

Applicant must have (and be able to document) ALL of the following qualifications:

• Hold a degree in "Clinical Research" from an Associate, Undergraduate, or Graduate Degree Program AND 

• Have completed a minimum of one year of full-time experience (or 1,750 hours part-time) during the past two years as a Clinical Research Professional

Category 3

Applicant must have (and be able to document) ALL of the following qualifications:

• Hold an Undergraduate or Graduate Certificate in “Clinical Research” with a curriculum of no less than 12 semester (credit) hours or totaling a minimum of 144 credit hours from an academic institution of higher learning (community college, college or university) AND

• Hold an Associate’s or Bachelor’s Degree in a science, health science, pharmacy or related field AND 

• Have completed a minimum of one year of full-time experience (or 1750 hours part-time) during the past two years as a Clinical Research Professional.

ACRP CCTI Certified ClinicPrincipal Investigator

The CPI® eligibility criteria define the minimum experience required before a PI can apply for the program. It is important to compare the CPI® eligibility criteria with your experience to self-determine your eligibility before submitting an application and payment. All applications must undergo a formal review process to determine an applicant’s eligibility to sit for the exam.

PI Certification Eligibility Requirements

In order to be deemed eligible to take the CPI® exam, applicants for the CPI® credential must be able to provide evidence through a job description, detailed CV or other documentation that they:

• Have a doctorate level degree and;

• Have proof of employment as a PI during at least two (2) of the most recent five (5) years and;

• Perform all of the essential duties as detailed below.

The PI Certification Handbook has complete employment definitions.

Update: The CPI Exam is the first exam being offered to all investigators with a doctoral-level degree. A license to practice medicine is no longer required.

NAIM CIM Certified IRB Manager

To qualify for the Certified IRB Manager Examination, you must meet the following
requirements:
     • Applicants must have a Bachelor’s Degree and 2 years of relevant IRB
      Management experience within the last 5 years.
      OR
     • An Associates Degree from a two year college or technical school and 2 years
      of relevant IRB Management experience within the last 5 years.

CCIP CIP Certified IRB Professional

Eligibility Requirements

This certification program is for individuals whose primary job responsibilities include substantial participation in overseeing, administering or performing the daily activities of an IRB as part of a HRPP. Individuals involved in IRB activities who meet the following eligibility requirements are eligible to take the examination: 

• A Bachelor's degree plus two years of relevant HRPP experience, completed on or before the first day of your chosen testing period (see front cover)

or

• Three years of relevant HRPP experience, completed on or before the first day of your chosen testing period

or

• Current certification as a CIP

RACC CRA Certified Research Administrator

Bachelor’s Degree and three (3) years of professional experience in research or sponsored programs administration either in a sponsoring or recipient organization or the equivalent in a self-funded organization;

OR

An Associate’s Degree and five (5) years of professional experience in research or sponsored programs administration either in a sponsoring or recipient organization or the equivalent in a self-funded organization;

OR

No degree and six (6) years of professional experience in research or sponsored programs administration either in a sponsoring or recipient organization or the equivalent in a self-funded organization. *

MAGI CRCP Certified Research Contract Professional

People often ask how to prepare for the exam. Two years of experience with a variety of negotiation partners may be sufficient to pass the exam. A careful reading of MAGI's Model CTA, Clinical Trial Agreement Handbook (Original), and Model CDA is helpful. There are numerous relevant articles in the Journal of Clinical Research Best Practices. Attending MAGI's Clinical Research Conference is good preparation, provided you attend sessions and workshops that address relevant topics where you need more knowledge. Sample questions, study guides, or other study materials are not available. However, imagine an exam for professional chefs. One question might be, "Describe the process of making an omelette." Another might be, "List five spices used in Chinese cuisine." Another might be, "What are the pros and cons of gas vs. electric stoves?"

RAPS RAC Regulatory Affairs Certification

The RAC is the only credential for regulatory professionals in the healthcare product sector. The RAC demonstrates to employers, clients and colleagues essential knowledge, critical thinking abilities and a commitment to continuing professional development. It is designed for working regulatory professionals, with at least three to five years of regulatory experience. There are six different RAC exams. The US, EU and Canada exams test regional regulations and involvement with regulatory bodies. The global exam focuses on international standards and guidelines. The devices and drugs exams have a global focus yet aligns to a specific sector of regulation knowledge. All six exams test for regulatory knowledge, critical thinking and analysis throughout the lifecycle of a product.

SQA RQAP Registered Quality Assurance Professional

The Society of Quality Assurance is proud to offer the professional credential Registered Quality Assurance Professional (RQAP) for professionals working in Good Laboratory Practices as well as for professionals working in Good Clinical Practices. Registration is a recognized standard of experience and knowledge throughout the QA industry, in the US and around the world.

What the credential demonstrates

• Proof of your knowledge of the regulations/guidelines and how they are applied

• Commitment to a high quality standard in the QA industry

• Personal professional growth and achievement

How it Works

1. Professionals must pass an examination in either Good Laboratory Practices or Good Clinical Practices to receive the RQAP credential.

2. Registered professionals must re-register every three years by submitting documentation of ongoing professional activities. These activities include, but are not limited to:

   • Attending the SQA Annual Meeting and/or Quality College

   • Attending events of SQA Regional Chapters

   • Attending events of relevant professional associations/societies, e.g. JSQA, RQA, RAPS, DIA, ACS, ACRP, NAICC, AALAS, etc. (See our MOU Organizations and Liaison Organizations.)

   • Completing courses in the SQA Online Learning Center

   • Attending SQA webinars or webinars offered by relevant professional organizations

   • Studying the SQA Annual Meeting Online Library

   • Participating in the SQA Mentoring Program

   • Writing test items for an RQAP exam

More on RQAP Re-registration

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CLINICAL RESEARCH TRAINING FOR NURSES

Guide to Becoming a Clinical Research Nurse

1. What is Clinical Nursing Research?

Nurses are known for providing direct care for patients. However, nurses may take up roles that are completely new to them within the world of clinical research. These roles include clinical research coordinator, educator and manager. They can also take up less traditional role like regulatory specialist, study monitor and IRB (institutional board review) admin.

• Regulatory specialist: their activities relate mainly with preparing regulatory documents and communicating with regulatory bodies. Nurses can work as a regulatory affairs specialist, a regulatory operation coordinator, or a regulatory coordinator. They can work within government agencies, pharmaceutical companies, academic medical centers.

• Study monitor: they monitor clinical research practices and make sure that it complies with necessary research protocols and regulations. They tend work at government agencies, biotechnology companies, pharmaceutical companies, contract research organizations, device manufacturers etc.

• Institutional Review Board (IRB) administrator: they are the professionals in charge of overseeing, administrating, implementing and managing IRB activities, like policies and procedures that relates to protecting human welfare. They can work at all IRBs: local, commercial or central IRB.

Nurses that have developed interest in the field of clinical research can join professional organizations. This provides them with the opportunity to network and continue their education through mediums like conferences, webinars, discussion groups, publications and online resources. These avenues serve as part of their clinical research training.

Certification is often a parameter used to measure professional expertise. This is based on criterion that reflects skill, knowledge, educational preparation, ability, and competence that are developed from experience in that area of specialization. Nurses that developed an interest in clinical research and have taken a clinical research training program have an opportunity to be certified through the:

• Society for Clinical Research Professionals, Inc. (Certified Clinical Research Professionals)

• Association for Clinical Research Professionals (Certified Clinical Research Associate or Certified Clinical Research Coordinator)

This field of clinical research gives nurses a chance, an opportunity to advance themselves professionally in a field that might not have been explored by them before. The benefits of having a registered nurse cover letter are insurmountable. This also provides a career path that can show family members the benefits of working in the medical field.

Nurses that have gone through the clinical research for nurses, otherwise called research nurse can carry out research on the various aspects of the human health, such as illness, pharmaceutical and health care methods and treatment plans. The main aim of this research is to improve the quality of health care service delivery. Helping patients and their family in a healthcare facility also brings a level of joy that is hard to find in many other career paths.

Roles of Research Nurses

• They are responsible for designing and implementing research studies.

• They observe procedures for treatment, collect and analyze data.

• They report their research results to appropriate quarters.

• They write articles and report their research findings in nursing or medical professional publications and journals.

• They help in recruiting participants for studies and are involved in providing direct care for the participants.

Clinical research nurse salary can make use of their communication skills as well as their critical thinking skills gotten from their knowledge and experience in healthcare to further their career in this exciting way.

Know that future CRNs can speak to our 24/7 chat and phone advisors to request information on partial scholarships and payment plans for nurses.

2. Clinical Research Nurse Salary

The average pay for a Clinical Research Nurse is $31.28 per hour.

MD Anderson Cancer Center Clinical Research Nurse salaries - $71,503/yr

Northwestern University Clinical Research Nurse salaries - $75,005/yr

NIH Clinical Research Nurse salaries - $77,331/yr

CLINICAL RESEARCH NURSE JOB Description

A clinical research nurse conducts scientific research on different aspects of human health like illnesses, pharmaceuticals, treatment plans and healthcare methods. Their major goal is to improve the quality of healthcare services that are administered to the patients.

3. How do I get Clinical Research Nurse Experience?

Experience don’t just jump on you, you have to get it by practice. CCRPS affords you an opportunity to acquire knowledge in clinical research, and not just knowledge but experience as well. Registering for the appropriate course will boost your knowledge base and as well you get experience of clinical research first hand.

As a clinical research nurse, you will be at the forefront of new medical discoveries, and help develop breakthrough cures and medical treatments. The work that you do during your career can help some patients live longer or better quality of life. You may be responsible for studying diseases and disorders, as well as developing new treatment plans. You will also help test new treatments and medications that could possibly change the way a disease or disorder is perceived.

The field of clinical research can be very rewarding and fulfilling. A good research nurse is dedicated to their work and ready to take on everything that the profession throws their way. If you’re looking to pursue a research nursing career, you should have an excellent understanding of the research process as well as the specialty area that you’re studying.

Excellent communication skills are also a must. You must be able to effectively communicate with scientists, physicians, researchers, patients, and corporate executives.

4. What Does a Clinical Research Nurse Do?

The duties of a research nurse will typically depend on their employer and role. Some research nurses may be responsible for studying diseases, while others may help create and improve new medications and other treatments.

clinical research nursing scope and Standards of Practice

Clinical research nurses can take up clinical research jobs in institutions like research organizations, pharmaceutical companies, universities, research laboratories, government agencies and teaching hospitals.

The work that a research nurse does is quite exhaustive and it includes;

• They use their knowledge of the basics of clinical research in designing and implementation of research studies.

• Observation of the procedures for patient treatment, collection and analyzing of data.

• They report their research findings to the relevant authorities. They may also have to present their results at health conferences and publish them in journals.

• They write grant applications in order to secure funds to carry out the research.

• They render assistance in the process of recruiting study subjects.

• They provide direct treatment for research participants.

Research nurses that study diseases and illnesses will often perform a great deal of research, both by studying previous findings and observing patients. They may be required to examine medical journals, for instance, as well as observe, study, and care for patients suffering from a particular disease.

They make decisions based on the observations made as to which patients are the best candidates for certain clinical trials. During clinical trials, the research nurse will administer medications or perform other treatment procedures, During this process, research nurses must closely monitor each patient’s progress. This includes documenting side effects, drug interactions, and the overall efficiency of the medication.

Aside from caring for patients, documenting and recording information during clinical trials are the most important responsibility that a research nurse has. The information and data gathered during the research must be compiled into reports and handed over to senior clinical researchers or specialists.

5. How Do I Become a Research Nurse?

Don’t expect to become a research nurse overnight. It's a lot of work and you are expected to undergo years of training and experience.

The clinical research nurse job is a competitive one and certificates are not just handed out to anybody. The conditions to be eligible to take the certificate exam is that you must be an experienced registered nurse and your experience must include having thousands of hours of experience in the area of clinical research.

How to Become a Registered Nurse (RN) in 2020 that contains everything a person pursuing a nursing job should know - responsibilities, education, salaries and more.

The first step toward becoming a research nurse is to obtain a proper education. You can start with a bachelor’s degree in nursing, although many employers prefer that their research nurses have master’s degrees or even doctoral degrees in their chosen specialty. During your schooling, classes in research and statistics are a must and are courses in your chosen area of expertise.

According to clinical research job websites, many research nurses have a MSN degree and some have a PhD in nursing. Many of them attain these degrees of education in order to give them an edge on getting clinical research positions. While studying, courses in statistics and research are mandatory.

There are two main certifications that clinical research nurses can get from the Association of Clinical Research Professionals (ACRP). You can get certification to become a certified clinical research associate or you can choose to become a certified clinical research coordinator.

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

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6. Clinical Research Nurse Requirements and Certifications & Nursing Cover Letter

A bachelor's degree in nursing does meet licensure requirements for graduates to become registered nurses (RNs), which qualifies individuals for the specialized certification. Bridge programs, such as an RN-to-Bachelor of Science in Nursing (BSN), require previous nursing education for admission. Nursing students complete traditional classroom courses, laboratory experiences, and a clinical practicum in a medical setting, which includes a hospital, assisted living facility, and long term care center.

For specific education in clinical research, trained RNs enroll in graduate certificate and degree programs. There students are introduced to case studies, ethical research practices, and financial matters affecting the design, implementation, and funding of clinical research trials. In a master's program, studies in research ethics point students towards ethical research practices, including a discussion on human rights, misconduct, and conflicts of interest. Graduate programs will also include quantitative research and a capstone project.

All RN-to-BSN programs will require an RN license to enroll. Master's and graduate certificates will need a bachelor's degree with sufficient prerequisite coursework in the field. In addition, they will need letters of recommendation or reference, a personal statement, and GRE scores.

Becoming a nurse researcher which is a highly specialized career requires an advanced degree and training in informatics and research methodology and tools. The initial step for these individuals, or for any aspiring advanced practice nurse, is to earn a Bachelor of Science in Nursing degree and pass the NCLEX-RN exam. Once a nurse has completed their degree and attained an RN license, the next step is to complete a Master's of Science (MSN) in Nursing program with a focus on research and writing. MSN courses prepare nurses for a career in research and usually include coursework in statistics, research for evidence-based practice, design and coordination of clinical trials, and advanced research methodology.

A TYPICAL JOB POSTING FOR A RESEARCH NURSE POSITION WOULD LIKELY INCLUDE THE FOLLOWING QUALIFICATIONS, AMONG OTHERS SPECIFIC TO THE TYPE OF EMPLOYER AND LOCATION:

• MSN degree and valid RN license.

• Experience conducting clinical research, including enrolling patients in research studies, Implementing research protocol and presenting findings.

• Excellent attention to detail required in collecting and analyzing data.

• Strong written and verbal communication skills for interacting with patients and reporting research findings.

• For a person to practice nursing legally, acquiring of nursing credentials and certifications is very important. For instance, some nurses who achieve a master's degree (MSN) leave the patient care aspect of nursing, and practice in a more managerial role.

CRA JOB OPPORTUNITIES

If you choose to become a Clinical Research Associate (CRA), you will have a key role in the success of clinical trials. Most CRAs have a nursing background, like yours. You will be the primary contact and support for trial sites, ensuring that the study is conducted according to the protocol, ICH-GCP, regulatory requirements and standard operating procedures (SOPs).

The Clinical Research Associates also offers you the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them.

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

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Speak to our 24/7 chat and phone advisors to request information on partial scholarships and payment plans for nurses.

Clinical research coordinators have the responsibility to oversee all daily activities of staff that are given the responsibility to conduct research. They have to do their work alongside principal investigators so as to make a determination of whether the study being conducted is viable or not. They also have to workout the budget at hand. They also need to make a review of all research protocols, making sure that all the test subjects know the protocols. They help in carrying out the research.

The Salary

When a clinical research coordinator is experienced, pay has quite an encouraging trend. If a clinicalresearch coordinator is a new entrant that has experience of less than five years, they earn a salary of around 43,000 dollars. This total is an average, according to salaries that were given by different anonymous users.

Usually, the compensation includes overtime payment, bonus payments, and even tips. In the mid of their careers, clinical research coordinators have experience of 5 to 10 years and they can expect a compensation of around 51,000 dollars. This is also an average that is based on different salaries submitted.

There is also the category of clinical research coordinators who have over 20 years’ experience in the field. For these professionals, the compensation is an average of 62,000 dollars and this is based on salaries submitted.

Clinical research coordinator salary by location

It is important to appreciate that different locations have different salary variations. There are some areas that pay more than the average, while others may pay less. If this is a career that you are willing to pursue, it is best that you find out as much as you can about the salary expected within your area. This information can help you negotiate for the best compensation for services rendered.

How to Become a CRA in Canada

1. How to Get A Clinical Research Associate Certificate Online in Canada

CCRPS offers Canadian CRA certification for students living and working in Canada. A CRA certification in Canada provides students with additional knowledge of resources and guidelines in order to work in clinical research.

Our certification specifically state and prove that you have reviewed Canadian guidelines in clinical research and meet the competencies required for all clinical research associates.While our certificate is accredited by the ACCRE, 4 other organisations, and shows employers you have the working knowledge to act as a CRA; the CRAC credentialing exam will help further establish your professionalism. If you already have experience as a clinical research associate, you can use this course to prepare and sit for the CRAC examination.

In order to become a certified Canadian CRA, you must take the CRAC credentialing examination. To sit for the examination, you must fulfill one of these requirements:

• 2 years of clinical research expereience within the last 5 years

• 3,500 hrs of part time experience with at least 1 year of Canadian experience within the last 5 years

• A post-graduate certificate in clinical research and at least 1 years’ experience over the past 2 years in clinical research. You must have at least 1 year of Canadian experience.

2. Clinical Research Associate Canada (CRAC) Membership

While CCRPS membership is free, you still benefit from obtaining CRAC membership even if you do not have enough experience to sit for the CRAC credentialing exam. Membership can create networking and job opportunities, as well as provide insight into the field. All interested professionals should become a Member of the Official Canadian CRA Association and list this involvement on their CV and cover letter.

3. CCRPS Canadian CRA Certification (CCRAC) for Resume Building

As we teach nearly 30 Canadian students each quarter, our Canadian Clinical Research Associate Certification will allow students to strengthen their application and resume, specifically towards Canadian guidelines and policies.

4. Landing A Entry Level Clinical Research Associate Job in Canada

Unfortunately, many professionals have trouble securing a job in order to get experience and take the CRAC exam. Our certification, specifically created for Canadian CRAs, provides entry-level science professionals with all the resources they need to be a working CRA in Canada. Our online exam can be taken at any time, if you enroll or demo our course.

5. Clinical Research Associate Programs in Canada

In addition to providing 130 modules, our CRA certification exam is priced affordably and the same as our American students. Students can gain valuable work experience by applying to be one of our CCRPS Clinical Research Education Fellows for a 1 month remote internship to develop and strengthen your resume.

6. Salary of Canadian Clinical Research Associate

Clinical Research Certification Specifically for Canadian CRAs

CCRPS offers one of the only online certifications specifically designed for entry-level and mid-level professionals in clinical research associate knowledge. We prepare you to understand and apply all skills required to secure a job in clinical research.

Want to Learn More About Clinical Research?

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