CCRPS Clinical Research Certificate Program Overview
CCRP CRRA Certified Clinical Researcher Associate
This program does not require more than a medical sciences education which includes FMGs, BSNs and bachelors graduates. The Clinical Research Associate Training Course is a 110 module course, taught by Senior CRA and Physician of 25 Years, Dr.Kamal. Dr.Kamal offers the training, experience, interviewing, letter of references and connections that you need to get a job supervising clinical research efforts. We provide clinical research associate training and job placement for nurses, science bachelor degree holders and international medical graduates.
For those interested in expanding their knowledge and skills, consider enrolling in the CRA or the Advanced Clinical Research Project Manager Certification courses for further specialization.
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 eligibility requirements, for the CCRA® program outline the experience that a CRA must have before applying for the program. It's crucial to assess how your career and education align, with these eligibility criteria before you submit your application and payment. All applications go through a review process to establish whether an applicant meets the requirements to take 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:
Stay out of the investigative staff who are conducting the research at the site or institution. This means they are not the PI or site manager's report and they can not change or manipulate data.
They work for the sponsor. Are hired to carry out a monitoring role for them.The sponsor could be a pharmaceutical or device company,a funding agency,a university department,a doctor and more.
Ensure you fulfill all the responsibilities outlined in the CCRA® certification for a specified duration of time which can encompass documented hours leading up, to the examination date and/or gained from past job roles depending on your educational qualifications.
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:
Make sure to carry out all the tasks outlined in the CRC guidelines for a minimum duration of hours needed.
The time spent carrying out the duties as a CRC may involve hours that have been recorded up to the examination date or, from work experience with the specific number of hours needed varying based on an individuals educational history.
For those pursuing a career as a Clinical Research Coordinator, the Clinical Research Coordinator course provides essential training and certification.
SoCRA CCRP Certified Clinical Research Professional
The candidate needs to adhere to the Good Clinical Practice (CMC guidelines while operating within the boundaries of protocols approved by IRBs, IECs or REBs or those that are specifically exempted.
The applicant must fulfil the following eligibility as stated here below. It should however be noted that the majority of the 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
Consider enhancing your understanding of GCP with the ICH-GCP course.
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 worked two (2) years of full time employment as a clinical research professional within past five years, you will NOT have to submit documentation supporting your educational experience.
Category 2
Applicant must have (and be able to document) ALL of the following qualifications:
From an associate, undergraduate, or graduate degree program, hold a degree in "Clinical Research".
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:
Earn a "Clinical Research" certificate, at the undergraduate or graduate level with a program that consists of a minimum of 12 credit hours per semester or totaling 144 credit hours from a higher educational institution (such, as a community college or university).
Hold an Associate’s or Bachelor’s Degree in a science, health science, pharmacy or related field.
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 state the minimum experience that a PI must have in order to apply for the program. It is suggested that you compare the CPI® eligibility criteria with your experience before you decide whether you are eligible to apply and pay for the exam. All applications are subject to a formal review process to determine if an applicant is eligible to take 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
Proof of employment as a Principal Investigator (PI) during at least two (2) of the most recent five (5) years.
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 to be offered to all investigators with a doctoral-level degree. It is no longer required that you have a license to practice medicine.
NAIM CIM Certified IRB Manager
To qualify for the Certified IRB Manager Examination, you must meet the following requirements:
2 years of relevant IRB and a Bachelor’s Degree must apply.
Management experience within the last 5 years.
2 years of relevant IRB Management experience within the last 5 years. An Associates Degree from a two year college or technical school
CCIP CIP Certified IRB Professional
Eligibility Requirements
This certification program is for people whose job responsibilities primarily involve significant involvement 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)
You should have three years of HRPP experience that is relevant, to the position, before the start of your selected testing period.
Current certification as a CIP
RACC CRA Certified Research Administrator
A 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.
An Associate’s degree and 5 years professional experience in research or sponsored programs administration, either in a sponsoring or recipient organization, or the equivalent in a self-funded organization.
No formal. Six years of work experience, in managing research or sponsored programs either at a funding organization or a receiving institution or the equivalent, in a self supported entity. *
MAGI CRCP Certified Research Contract Professional
People are always asking how to get ready for the exam. It could take two years of experience with different negotiation partners to pass the exam. It is helpful to read through MAGI's Model CTA, Clinical Trial Agreement Handbook (Original), and Model CDA carefully. There are many relevant articles in the Journal of Clinical Research Best Practices. It is a good preparation for the Clinical Research Conference of MAGI, if you pay attention to the sessions and workshops that are relevant for your needs, on topics where you need more knowledge. There are no sample questions, study guides, or any other form of study material. But then you can close your eyes and try to picture an exam for professional chefs. One question might be, ’How to make an omelette?’ Another might be, ’What are the five spices used in Chinese cuisine?’ Another might be, ’What are the pros and cons of gas versus electric stoves?’RAPS RAC Regulatory Affairs Certification
The RAC is the only credential for regulatory professionals in the healthcare product sector. Employers, clients and colleagues see that the RAC proves essential knowledge and a commitment to continuing professional development and well as critical thinking abilities. It is 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 knowledge of regional regulations and interaction with regulatory bodies. The global exam is designed to cover international standards and guidelines. The devices and drugs exams are a global focus, but align to a specific sector of regulation knowledge. Regulatory knowledge, critical thinking and analysis are tested throughout the lifecycle of a product in all six exams.
SQA RQAP Registered Quality Assurance Professional
The Society of Quality Assurance takes pride in providing the Registered Quality Assurance Professional (RQAP) credential to those, in the fields of Good Laboratory Practices and Good Clinical Practices, in the United States as a mark of their expertise and experience.
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
To receive the RQAP credential, professionals must pass an examination under either the Good Laboratory Practices or the Good Clinical Practices umbrella.
Every three years, registered professionals must re-register, by providing evidence of continuing professional activities in the form of documentation. 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
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