CCRP COURSE Reviews

Human testimonials from our students below

 


ADVANCED Clinical Research Associate Training and Placement

ADVANCED CLINICAL RESEARCH MONITOR TRAINING

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, you might get more chance with that.

Further certification can enhance your resume such as the ACCRE accredited CRA program which contains 110 learning modules for Clinical Research Associate Training and Placement

 

Clinical Research Associate Certification
1,495.00 1,795.00

Enrollment for the Online Clinical Research Training Program Available on Blackboard

- 110 modules + examnination

-Tutoring for modules and final exam includes

- Full online certification by ACCRE (same accrediting body for SOCRA/ACRP)

- Next day access to all course modules

- Modules available at student pace via Blackboard Online 24/7

- Ability to finish course and certification at your own time (some finish in a week, others in a few months)

- Job placement and recruitment help with our Aerotek partners

Course certification after completion of all 110 modules and competency exam with a score above 75% is provided.

Quantity:
Enroll

 


Clinical Research MONITOR Training

Clinical Research Associate Certification
1,495.00 1,795.00

Enrollment for the Online Clinical Research Training Program Available on Blackboard

- 110 modules + examnination

-Tutoring for modules and final exam includes

- Full online certification by ACCRE (same accrediting body for SOCRA/ACRP)

- Next day access to all course modules

- Modules available at student pace via Blackboard Online 24/7

- Ability to finish course and certification at your own time (some finish in a week, others in a few months)

- Job placement and recruitment help with our Aerotek partners

Course certification after completion of all 110 modules and competency exam with a score above 75% is provided.

Quantity:
Enroll

clinical research MONITOR training

While several careers exist with a science degree, the best exposure to a medical career with a science bachelors is through Clinical Research Training. This can be taken as early as your senior year of college to prepare for a job directly out of university.

CRA positions right out of undergrad are nearly impossible to get due to the yearly 1.9 million graduates of science degrees (and approximate 2,000 applications per position). This is why Clinical Research Training is an essential investment in your career.

CRA positions after hiring will cover the expenses of travel, housing, food, and more if visiting clinical sites. Most pay $6.5-12k a month with the potential to move on to a CRA position after 2 years.

While many positions will fund or reimburse your CRA training; securing an initial position is the tough part. This is why our Clinical Research Training provides 110 clinical research training modules and interview preparation with a Senior CRA and Physician of 25 years.

Our Clinical Research Training makes almost anyone interested in making use of their science degree in medicine possible. We take on students with no medical background to full-on doctors looking for a better position due to their international medical degree.

We also offer private Principal Investigator Training for practicing physicians.

See available positions here to understand why CRA certification is essential to obtaining a career in medicine with a science degree.


 

Clinical Research Training for Nurses

Nurses are known to be the ones who provide direct care for the patient. Some nurses are also familiar with the role of nurse scientist. 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 or 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 regulatory affairs specialist, regulatory operation coordinator, regulatory coordinator. They can work with 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 can also 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. The activities could be policies and procedures that relates to protecting the welfare of humans. They can work at all IRBs, local, commercial or central IRB.

Nurses that have developed interest in the field of clinical research can associate with professional organizations, this provides them with the opportunity for networking and option to 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 a particular criteria that reflects skill, knowledge, educational preparation, ability and competence that are developed from experience in that area of specialization. Nurses that developed interest in clinical research and have undergone a clinical research training program can have an opportunity to be certified through the:

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.

Nurses that have gone through the clinical research training, 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.

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.

Nurses 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.

Our course allows new and current nurses to become certified to work as CRCs/CRMs/CRAs and nurse researchers with no prior experience.

Clinical Research Associate Nurse Certification
1,495.00 1,795.00

- 110 modules

-Tutoring for modules and final exam includes

- Full online certification by ACCRE (same accrediting body for SOCRA/ACRP)

- Next day access to all course modules

- Modules available at student pace via Blackboard Online 24/7

- Ability to finish course and certification at your own time (some finish in a week, others in a few months)

- Clinical research training developed for physicians and healthcare providers

- Job placement and recruitment help with our Aerotek partners

Course certification after completion of all 110 modules and competency exam with a score above 75% is provided.

Enroll

 


 ICH GCP CERTIFICATION

ICH is the abbreviation for International Conference on Harmonisation of technical requirements for registration of pharmaceuticals for human use. The ICH is an international body that sets the standard which becomes regulations for clinical trials involving human subjects. The ICH sets the standard that defines the guidelines for Good Clinical Practice (GCP).

GCP is an international standard that ensures that ethical and scientific qualities are maintained in the designing, recording and reporting of clinical trials involving human subjects.

The aim of this regulatory standard is to ensure that the well-being, right and safety of the human beings recruited for clinical trials are protected. It also aims to ensure that data gotten from clinical trials are accurate, reliable and credible, irrespective of wherever or whatever clinical research facility that the trials are being conducted in the world.

ICH GCP certification is a formal recognition of an individual's knowledge and competence in their ability to carry out applicable GCP guidelines under different circumstances.

It is important for all professionals in the clinical research industry to get the much needed training in Good Clinical Practice (GCP) and be certified as well. As a matter of fact, most companies now take measures to ensure that their staff are GCP certified. Being GCP certified has become a minimum requirement for anyone who would like to explore a career in the area of clinical research.

Although all clinical research professionals are required to be GCP certified, GCP certification is of more importance to the following individuals:

It is highly recommended all over the world to get the Good Clinical practice (GCP) training and certification if you are a clinical research professional or you are aspiring to be one. That is the least acceptable standard to work in the clinical research industry. Beyond GCP certification being a required minimum for a clinical research professional. There are a few other reasons why you need the GCP certification. They include:

  • It is a global formal acknowledgement of an individual's professional eligibility to work as a clinical research professional.

  • In order for organizations involved in the business of clinical research to comply with the laid down industry guidelines and regulations, Good Clinical Practice (GCP) training is important for members.

  • GCP training equips the participants with the knowledge of the regulations that are applicable in clinical research.

  • Pharmaceutical and biotech companies, as well as contract research organizations recommend that their employees are GCP certified.

ICH GCP in today's clinical research world is now more important than ever. The evolution of medical science and the complexities of research process highlight the importance of guidelines that ensure that clinical research are carried out properly.

CCRP’s online ICH GCP certification course can be completed in 2-3 days online to receive ICH GCP certification for your current job or future job. It is required in many fields in order to conduct clinical trials and we offer an in-depth overview of ICH GCP through our module course.

Our ICH GCP certificate is compliant with 2019 ICH GCP protocol and accredited by the Accreditation Council For Clinical Research & Education; the only major accrediting body for clinical research education.


ICH GCP Certification
100.00 280.00

ICH GCP Certification

ICH-GCP is the guideline ruling all clinical research including its conduct, performance, monitoring and reporting of the results. This online certification focuses on the requirements of Good Clinical Practice (GCP) in clinical studies with pharmaceuticals. The certificate is accredited by the ACCRE and CCRP.

-Next day access to certification modules

-16 modules + exams

-ICH GCP Certification

Quantity:
Enroll

 

Clinical Trial Assistant Training

The work of a clinical trial assistant in the set up of a clinical research can never be overstated. It is an important job that requires a whole lot of interest in order to be successful as one. If you have developed interest in becoming a clinical trial assistant, there are certain questions that you must ask yourself. Are you really cut out for this career path? Can you ensure that your availability during the duration of a research from start till its completion, to monitor the trial subject and ensure that the trial is conducted in a safe and ethical manner? Are you eager to take up more responsibilities in a work place? If your answers to this questions are yes, then you might just be cut out for the job of a clinical trial assistant.

A clinical trial assistant or clinical research associate have a lot of responsibilities and roles to fulfil within a clinical research institute to ensure the success of a clinical research. Some of these responsibilities include:

  • They are responsible for maintaining the standard operating procedures (SOP).

  • It is their duty to provide regular report updates of the progress of clinical studies to the appropriate personnel.

  • They are involved in the planning and conducting of pre-study site evaluation.

  • They conduct clinical site feasibility and are as well involved in study visibility.

  • They assess the study subjects to ensure that the appropriate clinical protocols are observed and the trial is in sync with laid down regulations.

The minimum educational requirement for an entry level job as a clinical research associate is an undergraduate degree in health sciences related courses like nursing, life sciences, medical science, biotechnology etc. A diploma in clinical research from a reputable clinical research institution is also another way to go. But graduate degrees offer more benefits and opportunities like a higher pay, eligibility for senior positions etc.

Another avenue through which you can become a clinical trial assistant is through the administrative side. This is possible and is most common for people without formal education in the fields mentioned. It is however a tasking work and very demanding as it requires a lot of administrative knowledge in the area of clinical research.

To be successful as a clinical research associate, there are certain skill sets that are required.

  • A knowledge of the challenges and restrictions involved in the implementation and retention of databases.

  • A complete understanding of the responsibilities and liabilities involved in the use of humans for trial tests.

  • An ability to make excellent clinical development plan.

  • Must be able to ensure that data gotten from clinical trials are accurate and reliable and the legal rights and privacy of the subjects are protected.

Having these above listed skills and being efficient in them make the job of a clinical trial assistant easier and more interesting.

Clinical research associates can work in several kind of organizations including:

  • Clinical research organizations (CRO)

  • Pharmaceutical companies

  • Biotechnology companies etc.

Becoming a clinical trial assistant does not require much. If you're interested, get a degree in the required field and then apply afterwards to increase your chance of success.

CCRP offers complete clinical trial assistant training and certification by the ACCRE through our clinical trial assistant training course. Enroll below:

Clinical Trial Assistant Training
500.00

Enrollment for the Online Clinical Research Assistant Training Program Available on Blackboard

- 40 Clinical Research Assistant Training Modules with ICH GCP Certification

- Certification as a Clinical Trial Assistant by the ACCRE

- Next day access to all course modules

- Modules released based on student pace

- Ability to finish course and certification at your own time (usually less than 1 week)

- Clinical trial assistant training with no prior experience required

- Job placement and recruitment help with our Aerotek partners

Quantity:
Enroll

 

 

 

ONLINE CLinical research courses

 
Clinical Research Associate Certification
1,495.00 1,795.00

Enrollment for the Online Clinical Research Training Program Available on Blackboard

- 110 modules + examnination

-Tutoring for modules and final exam includes

- Full online certification by ACCRE (same accrediting body for SOCRA/ACRP)

- Next day access to all course modules

- Modules available at student pace via Blackboard Online 24/7

- Ability to finish course and certification at your own time (some finish in a week, others in a few months)

- Job placement and recruitment help with our Aerotek partners

Course certification after completion of all 110 modules and competency exam with a score above 75% is provided.

Quantity:
Enroll
ICH GCP Certification
100.00 280.00

ICH GCP Certification

ICH-GCP is the guideline ruling all clinical research including its conduct, performance, monitoring and reporting of the results. This online certification focuses on the requirements of Good Clinical Practice (GCP) in clinical studies with pharmaceuticals. The certificate is accredited by the ACCRE and CCRP.

-Next day access to certification modules

-16 modules + exams

-ICH GCP Certification

Quantity:
Enroll
Clinical Research Associate Nurse Certification
1,495.00 1,795.00

- 110 modules

-Tutoring for modules and final exam includes

- Full online certification by ACCRE (same accrediting body for SOCRA/ACRP)

- Next day access to all course modules

- Modules available at student pace via Blackboard Online 24/7

- Ability to finish course and certification at your own time (some finish in a week, others in a few months)

- Clinical research training developed for physicians and healthcare providers

- Job placement and recruitment help with our Aerotek partners

Course certification after completion of all 110 modules and competency exam with a score above 75% is provided.

Enroll
Clinical Trial Assistant Training
500.00

Enrollment for the Online Clinical Research Assistant Training Program Available on Blackboard

- 40 Clinical Research Assistant Training Modules with ICH GCP Certification

- Certification as a Clinical Trial Assistant by the ACCRE

- Next day access to all course modules

- Modules released based on student pace

- Ability to finish course and certification at your own time (usually less than 1 week)

- Clinical trial assistant training with no prior experience required

- Job placement and recruitment help with our Aerotek partners

Quantity:
Enroll
 

 

 

Principal Investigator Training

CCRP offers online principal investigator training to physicians and doctorate-level degree holders interested in beginning a career as a PI. The principal investigator training course is a 1-on-1 course designed to assist in obtaining the knowledge needed for initial PI roles. Because US PI certification requires at least 6 months of experience as a principal investigator, physicians in our online principal investigator training program seek this course to assist in their preliminary positions as a PI prior to the national PI certification exam.

 
 
clinical research training

60 hours

Our 60 hour principal investigator training course is designed to be one of the highest-density courses in the industry for principal investigators. Obtaining 60 hours of training on a 1-to-1 basis allows for doctorate-level degree holders to gain fundamental skills to secure a position as a principal investigator. This also ensures the basis of the online course to be beyond that of broad concepts, and tailors to each student’s needs in applying the concepts.

Online, self-paced

CCRP offers online, self-paced modules for principal investigators because we understand the demand of current jobs, research internships, board-certification exams, and family that can impact learning. While these modules are self-paced, all principal investigators are monitored daily by our Senior PI instructor to ensure adequate speed and retention.

 

 

Clinical Research Training

Designed For Nurses, Physicians, and Science Graduates To Earn The Knowledge of A Senior Clinical Research Associate In 30 Days with Clinical Research Training Online.

CCRP Course has successfully trained over 1,000 students through our instructors. Our lead instructor, Dr.Kamal T Dhaliwal has worked in the industry for over 25 years. In this time, she alone has lead education efforts for Clinical Research Training for many companies. With a background in education, the modules produced by our Senior Clinical Research team educate students up to the Senior Clinical Research Associate level regardless of current background. This has allowed clinical research training students to surpass the need for further training once hired, allowing for quicker promotions and hiring.

Unlike institutes which offer several types of training costing upwards of $7,000 to get up to the Senior Clinical Research Associate education, our single Clinical Research Training course trains all students up to this level. Most importantly, it provides access to students with less than the required 2 years of clinical research monitoring experience to become certified in the industry and secure their first job. In Clinical Research Training, students choose our course due to gaining 1-on-1 access to 110 clinical research training modules, and intensive training that can be completed in 30 days (and sometimes less). This allows students to choose the pace they want to enter the new industry and also complete the course online while working, studying for licensing exams, or waiting for residency/medical school entry.

 
 
clinical research training online

Travel or Work Remote

While 90% of our students are physicians (MDs, MBBS, IMGs), many students find a position paying more than they expected. Their favorite part of the position is being able to choose to travel (expenses covered) or work remote.

 

Clinical Research Training for Science Graduates

Science graduates with a bachelors, masters, or PhD in science fields often look into Clinical Research Training in order to advance their career. Working as a clinical research associate is one step up the ladder compared to an assistant or conducting the trials yourself. Rather than conducting the trials, you are put in charge of several trials in many medical hospitals, schools, and pharmaceutical labs around your region. The companies place priority on their staff for promotion which is why there is a 33% chance of promotion in the first year. Premed students in their gap year prior to medical school choose the Clinical Research Training route to get relations with admissions and faculty of medical schools while earning over $60,000 a year. Students with a masters of PhD are seeking the option to earn over $100,000 a year in a field that fosters a similar amount of discovery and exploration as their programs. Clinical research jobs offer this opportunity as well as the ability to transfer into management positions in the pharmaceutical and medical industry.

Clinical Research Training for Nursing Graduates

RNs and BSNs looking to enter the management field without excess on-floor or heavy-duty hours look into clinical research training as the next step. While 90% of our students are physicians, more than half of the clinical research associate workforce are former nurses. The position allows nurses to early more while working in a job with less demanding hours. Clinical research associates are commonly nurses because of their prior medical experience and many companies look to hire while keeping this background in mind. Many companies look for nurses also because of their attention to detail which is needed in the high-stakes field of clinical research where observation of trials and data is key. Because we provide up to the Senior level of clinical research training, nurses do not need further certification to be promoted if they are already in the field.

Clinical Research Training for Physicians (MDs, MBBS, IMG, FMGs)

90% of our students are physicians who are trained US medical graduates with or without residency, MBBS graduates, International Medical Graduates, and Foreign Medical Graduates. Many physicians choose to switch to clinical research because physicians are quickly hired and promoted along the pharmaceutical or medical institution they work for. Physicians who are taking the USMLE work as CRAs during their waiting year(s) in order to work in a job that pays enough to save, support their family, or give them enough time to be with their family by working remote. Physicians who were unable to find residency also choose this path because clinicians are treated as doctors in this field when monitoring and can still hold their MD title while working. Further, no physician is considered over-qualified for this position as most will be promoted to Senior CRAs within the first year. This can also be the best option to earn over $100,000 with a career more flexible and less demanding than many physician careers. Many physicians choose to enter the management sector as COOs, CEOs, and company executives after their first few years.

 

 

 

I Have A Degree In Science/Medicine. Now What?

We cover all the common questions our bachelors graduates ask when desiring a medical career with a bachelors degree.

DO I NEED A MASTERS TO GET A JOB WITH MY SCIENCE DEGREE?

A masters is an option many science degree holders take but it not always the best bet. Now, many masters science degree holders apply for jobs but are still placed in a lab and in a work environment they do not see growth in. A masters will only further your position in the lab, and less so in a career with potential. The best option is to consider a thorough Clinical Research Training course that can establish the experience and clinical research training needed to be hired, succeed, and advance in a medical-focused science career.

ARE THERE COURSES AFTER MBBS IN USA?

Many MBBS or foreign medical graduates opt to not take the USMLE or finish residency again but still desire a medical job with a similar amount of professionalism and recognition. A CRA position is the best next step after an MBBS in the US to work as a medical professional alongside many doctors who you will actually supervise and have equal-level relationships with. We offer advanced training for CRA certification for this very purpose. In fact, 20% of our Clinical Research Training graduates are MBBS holders, many others are IMGs.

WHAT SCIENCE DEGREE JOBS ARE IN DEMAND?

When you look for science degree jobs; most of them are in the lab actually conducting trials whereas a CRA supervises and reports them. If you want to apply your science degree without the manual labor of pipets and syringes, a CRA position can establish your footing in medical-leadership roles with your Clinical Research Training.

ARE THERE REMOTE JOBS FOR SCIENCE DEGREE HOLDERS?

The best known remote jobs for science degrees are CRAs after getting Clinical Research Training. You can work from home making $6.5-12k a month while having your internet, cell phone, printing, and laptop expenses reimbursed.

ARE THERE TRAVELLING JOBS FOR SCIENCE DEGREE HOLDERS?

Feel like you haven’t seen enough of the world because of studying so much in undergrad? CRA’s have the option to travel 100% with food, housing, and travel covered. You can choose which sites you want to travel to and arrive early to explore the cities and countries even more after Clinical Research Training.


 

 

Clinical Research Certification

Receive more information about the course by signing up below:

ICH GCP TRAINING 

The ICH GCP training modules go over the entire ICH GCP guidelines in detail. They teach you how to apply them rather than just understand the protocols. This is the essential basis of Clinical Research Training.

15 MODULES

1.   An Introduction to Clinical Research

2.   An Overview of ICH GCP

3.   Code of Federal Regulations

4. FDA 21 CFR Part 11 ( Part 1 and 2)

5. ICH GCP E6 Section 5 - Sponsors Responsibilities

6. ICH GCP E6 Section 4 - Investigators Responsibilities

7. ICH GCP E6 Section 4 - Investigators Responsibilities – Informed Consent Form

8. Reporting Responsibilities of the Investigators

9. Ethics of Research Involving Children

10. Ethics of Research Involving Mentally Incapacitated

11. Ethics of Research Involving Pregnant Women and Fetuses

12. Ethics of Research Involving Prisoners

13. ICG GCP 5.5 Trial Management – Data Handling and Record Retention

14. ICH GCP E6 and E2A - Adverse Events

15. Safety of Human Subjects in Clinical Research

Reference Modules - to be used for reference purposes only:

a) Common Terminology Used In Clinical Research

b) Commonly Used Abbreviations and Terms in Clinical Research

 

QUALITY MONITORING 

The quality monitoring modules are needed to work as a supervisor on clinical trials. This is the section not available in any other entry or introductory clinical research training course with more detail than many new Senior CRAs know. These modules allow you to obtain the application, examples, and guidelines needed to monitor trials with ease in your new position.

45 MODULES

1.    Duties and Responsibilities of a Clinical Research Associate

2.    Designs of Clinical Trials

3.    Phases of Clinical Trials

4.    Pre-Clinical Trials

 5.    Stakeholders in Clinical Research and Their Relationships

 6.    Contract Research Organization- CRO

 7.    Randomized Controlled Trials

 8.    Types of Monitoring Visits

 9.    Site and Investigator Selection

 10. Site Qualification Visit

 11. Routine Monitoring Visit

12.  Monitoring Tools and Notes

 13.  Checklists for Pharmacy Monitoring and Inspection Visits

14.  Site Close Out Visit

 15.  Source Documents

 16.  Inclusion Exclusion Criteria in Clinical Research

 17.  Interactive Voice Response System - IVRS

 18.  Protocol in Clinical Research

 19.  Protocol Deviations and Violations

 20.  Institutional Review Board

 21.  Quality Control in Clinical Research

 22.  Data Safety Monitoring board- DSMB

 23.  An Overview of Remote Monitoring

 24.  Centralised Versus Onsite Monitoring

 25.  Electronic Data Capture and Remote Data Capture Basics

 26.  Remote Monitoring of Clinical Trials and EMRs

 27.  Blinding in Clinical Trials

 28.  Communication between Blinded and Unblinded Staff

 29.  Investigational Product Storage and Dispensing

 30.  Investigational Product Accountability in Clinical Trials

 31.  Adverse Drug Reactions

 32.  Basics of Adverse Event Monitoring

 33.  Adverse Event Reporting

 34.  Risk Based Monitoring

 35.  Pharmacovigilance (Part 1)

36. Pharmacovigilance (Part 2)

 37. Safety Reporting Requirements for Sponsor Investigators

 38.  Investigator Initiated Multi Center Trails

 39.  IND and NDA Process

 40.  Guidelines for Designing and Completing Case Report Forms

 41.  Do’s and Don’ts of a Case Report Form Design

 42.  Introduction to Bioresearch Monitoring (BIMO)

 43.  Clinical Trial Management System-CTMS

 44.  Minimising Source Data Queries in Clinical Trials

 45. Role of Local and Central Labs in Clinical Trials

REGULATORY TRAINING  

Regulatory training allows you to understand and apply the FDA regulation guidelines to each individual trial you will supervise after your Clinical Research Training.

15 MODULES

1.    Regulatory Documents in Clinical Research

 2.    Regulatory Affairs

3.    Essential Regulatory Documents Guidance and Binder Tabs -Part 1

 4.    Essential Regulatory Documents Guidance and Binder Tabs - Part 2

 5.    Electronic Regulatory Submission and Review

 6.    Financial Disclosure- Duties and Strategies for Clinical Studies

 7.    Financial Disclosures and Conflicts of Interest in Clinical Research

 8.    FDA Form 1572 - Part 1

 9.    FDA Form 1571 - Part 2

10.  Delegation of Authority Log – DOAL

11. Investigators Brochures

12. Protocol Continuing

13.  IND Application

14.  Trial Master File Reference Guide

15.  Trial Master File and DIA Model

AUDIT AND INSPECTIONS  

The auditing and inspections modules train you to prepare clinical trials for auditing by your company, government organisation, or academic organisation after your Clinical Research Training.

SUBJECT RECRUITMENT, RETENTION AND COMPLIANCE 

5 MODULES 

1.    Compliance Requirements in Clinical Trials

 2.    Subject Recruitment and Retention (Part 1 and Part 2)

 3.    Increasing Subject Compliance in Clinical Trials

 4.    Ethical Consideration Associated with Investigator Payment and Patient Recruitment

 5.    Advertisement aid in Subject Recruitment and Retention6 MODULES

1.    Audits and Inspections in Clinical Trials

 2.    FDA Warning Letter

 3.    Site FDA Audit Inspection Checklist

 4.    How to Survive Through an FDA Inspection

 5.    Do and Don’ts during an FDA Inspection

 6.    Mock FDA Audits

MISCONDUCT AND FRAUD 

2 MODULES 

1.    Scientific Misconduct in Research and How to Prevent It

 2.    Misconduct in Research – Detecting Falsification

WRITING QUALITY MONITORING REPORTS & FOLLOW UP LETTERS

These modules immerse you in understanding, applying, and learning to write monitoring reports, follow up letters, and professional write-ups required in the CRA position after each clinical site visit or review after your Clinical Research Training.

16 MODULES

1. Site Monitor Transition Letter   

2. Checklist of Activities for Pre-Study Visit Qualification

 3.   Pre-study Visit Assessment and Monitoring Questionnaire

 5.   Pre-Study Visit Follow Up Letter

 6.   Site Initiation Visit Agenda

 7.   Site Initiation Visit Confirmation Letter

 8.   Site Initiation Visit Report

9.   Site Initiation Visit Follow Up Letter

10. Site Monitoring Visit Confirmation Letter/Fax

11. Site Monitoring Visit Report

12. Site Monitoring Visit Follow Up Letter

13. Site Close Out Visit Confirmation Letter

 14. Site Close Out Visit Agenda

 15. Site Close Out Visit Report

 16. Site Close Out Visit Follow Up Letter

COMPETENCY TESTING FOR A CRA   

The competency testing of your Clinical Research Training modules is the next step needed to ensure that you are ready for your interviews. We establish our CRA’s as future leaders in the clinical trial industry by ensuring you have the full education needed to be promoted in your career quicker than without the course.

Clinical Research Associate Certification
1,495.00 1,795.00

Enrollment for the Online Clinical Research Training Program Available on Blackboard

- 110 modules + examnination

-Tutoring for modules and final exam includes

- Full online certification by ACCRE (same accrediting body for SOCRA/ACRP)

- Next day access to all course modules

- Modules available at student pace via Blackboard Online 24/7

- Ability to finish course and certification at your own time (some finish in a week, others in a few months)

- Job placement and recruitment help with our Aerotek partners

Course certification after completion of all 110 modules and competency exam with a score above 75% is provided.

Quantity:
Enroll

Certified Clinical Research Professionals

Clinical Research Training Online

Welcome to CCRP

Certified Clinical Research Professionals is led by Senior CRA and Physician of 25 years, Dr.Kamal T Dhaliwal. Our team of CRAs, CRCs, physicians, and onboarding staff welcome you to one of the most in-depth courses for clinical research available. We offer clinical research training for physicians, international medical graduates, nurses, and healthcare providers. We offer clinical trials assistant training to high school students and graduates. All programs are self-paced and students can earn their clinical research certification online.

CCRP is known for our clinical research online training for Clinical Research Associates (CRAs), Principal Investigators (PIs), Clinical Research Monitors, Regulatory Affairs, ICH GCP Protocol, Clinical Quality Management and other crucial clinical research purposes, CCRP Clinical Training’s strategy provides students with self-paced online training experience based on core competency accredited by the ACCRE.

As educators in clinical research training, CCRP Clinical research training programs vary based on student’s location, time, and learning demands. These self-paced online modules, interactive tutoring sessions, or online monitored competency examination, CCRP clinical training provides a clinical research fast track approach to getting hired in clinical research.

CCRP Clinical training is able to provide large-group online training options for clinical research professionals and CROs globally. It is widely known for its comprehensive education and training programs. CCRP clinical training helps clients improve their programs by enhancing staff knowledge via its extensive online course and examinations.

 

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CCRP focuses on improving the training and adequacy of clinical research monitors around the world. Our goal is to provide thorough and detailed training to students from various backgrounds and help them to enter the industry. Contact CCRP Course regarding partnerships, questions, group pricing, and work opportunities.

Certified Clinical Research Professionals Society® Copyright 2019

Certified Clinical Research Professionals LLC.® Copyright 2019

Text Fax Call

833-222-2775

Headquarters

3911 Concord Pike #8030, SMB 6416 Wilmington, DE 19803

 

 

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Remote internships offered to select Clinical Research Training Students

Enroll for our clinical research training internship and/or our course by selecting your schedule first. Internships are remote and offered on a month-to-month basis for students. Courses allow for internships after Clinical Research Training completion.

Clinical Research Training Internship

We are not accepting further interns at this time

CLINICAL RSSEARCH INTERNSHIPS AVAILABLE NATIONWIDE. (outside of CCRP; make sure to include cover lever)

If you have a clinical research background but are having difficulty securing a new position please apply below for our CCRP Course Clinical Research Training Internship. Clinical Research Training internship opportunities are available to 15 students each month to help advance your career. We suggest the internship path for CRAs who are looking to transition to a management role, senior CRA role. We also suggest the Clinical Research Training internship for students who have taken other CRA certification courses but have not secured a position. All Clinical Research Training internship opportunities are remote and require a minimum of 8 hours a week. Clinical Research Training Internship completion includes employee reference, a letter of recommendation, and access to a Senior CRA for any questions and guidance.