Online Clinical Research Certification & Training Programs
Browse our leading course catalog to discover the most advanced, accredited clinical research training programs — fully online and self-paced. Chat with advisors 24/7 below.
Novel Clinical Research Courses for 2025 with Unmatched Curriculum & Support
Certificates
Start or advance as a CRC with our leading triple-accredited, 100% online, self-paced clinical research coordinator certification and training program —112 advanced topics for 2025, live webinars, mentorship, earn certificate and LinkedIn badge, and
$500
Certificates
Start or advance as a CRA with our leading triple-accredited, 100% online, self-paced clinical research associate certification and CRA training program —288 advanced topics for 2025, live lectures, mentorship, earn a certificate and LinkedIn badge,
$500
Certificates
Pharmacovigilance Certification - Advanced Pharmacovigilance and Regulatory Affairs Safety Certification (APRAC) ACCRE Accredited I 169 Lessons I Online I Instant Enrollment I Globally Recognized I 4 Wk Certification
$500
Certificates
Start or advance as a Research Assistant with our leading, triple‑accredited, 100% online, self‑paced research assistant certification and training program—114 advanced topics for 2025, live webinars, mentorship, 8 years of alumni success, earn your
$433
Certificates
Advance your career as a Clinical Research Project Manager, Trial Director, or Clinical Trial Manager with our trusted, triple‑accredited, 100% online, self‑paced 2025 certification program. Enjoy comprehensive clinical research director training and
$533
Certificates
Advance your career as a Medical Monitor or Medical Science Liaison with our trusted, triple‑accredited, 100% online, self‑paced certification and training program for 2025—master 250 in‑depth topics via live webinars and expert mentorship, join 8 ye
$533
Certificates
Master trials and improve outcomes as a Principal Investigator or Clinical Research Physician with our triple-accredited with CME, 100% online, self-paced Research Principal Investigator Training Program for 2025. Master 284 role-specific topics
$500
Certificates
Advance your expertise with our 100% online, self‑paced ICH GCP training program for 2025—utilized by leading voices in clinical trials. Master E6 (R3) training in 70 comprehensive lessons, with live webinars, expert mentorship, and hundreds of real-
$200
Certificates
CCRPS Clinical Research Community - Join Our New Convenient WhatsApp Group
Accredited by ACCRE, PIMED/JA for CME (AMA, ANCC, ACPE), and CPD, as well as recognized by TransCelerate Biopharma for Good Clinical Practice (GCP). Partnered with NHA. Exempt Vocational Training Programs are acknowledged by CO DOE.
Thousands of graduates are excelling in clinical research jobs globally (just check LinkedIn). Case study interviews reported increased job interview success, faster promotions, and enhanced professional competence.
Enjoy lifetime access to our constantly updated content, now enhanced with 600+ new interactive lessons for 2025. Access 24/7 support, join free weekly live sessions, and benefit from one-on-one mentorship for ultimate career guidance.
CCRPS programs are utilized by students from 1,200+ organizations, 7 government agencies, and 308 universities, resulting in graduates working at over 1,600 companies.
Learn on the go with mobile-friendly interactive lectures. Self-paced with instructor guidance. Complete your training online with 24/7 support, live sessions, one-on-one mentorship, flexible payment plans, and a 14-day refund policy.
CCRPS offers cutting-edge training with multi-specialty curriculums, expert skills, live sessions, and mobile-friendly learning. Our 2024 graduate survey confirms unparalleled career success.
View CCRPS Reviews
Explore the real-world impact of our clinical research courses. Scroll below to discover the top companies and job positions secured by our alumni.
"From IMG to Clinical Research Coordinator at Columbia University. This course exceeded my expectations with its thorough curriculum and insightful modules." – Lisa-Pierre
Companies: AstraZeneca, Sloan Kettering Cancer Center, US VA, Cedars-Sinai, Mayo Clinic, Apex Mobile Research, Prestige Medical, University of Alabama, Stony Brook Medicine, NYU Langone Health, Memorial Medical Center, Nova Research Institute, Quest Diagnostics, Nestle, Arizona Liver Health, King Hussein Cancer Center, NextStage Clinical Research, Janssen, Thermo Fisher Scientific, NewYork-Presbyterian Hospital, Impact Health & Research.
Job Roles: Clinical Research Coordinator, CRC II, Lead CRC, Senior CRC, Oncology Research Coordinator, Clinical Study Coordinator, Clinical Research Data Coordinator, Clinical Research Nurse, Clinical Director/Office Manager, Regulatory Contact, Clinical/Regulatory Coordinator, Clinical Trials Specialist, Research Regulatory Specialist, Certified CRC, Clinical Research Specialist, Sr. Director of Clinical Operations.
"From IMG to Clinical Research Coordinator – the hands-on activities solidified my understanding of complex concepts." – Umber Mahmood
Companies: University research groups, hospitals, clinics, clinical trial sites, pharmaceutical companies, government agencies (FDA, NHS, ICON PLC, PPD, IQVIA, Parexel, Johnson & Johnson, Medtronic, Novartis, Novo Nordisk, UNC Health, NYU Langone, Colorado State University, Baylor, Kaiser, Cornell, Boston University).
Job Roles: Research Assistant, Lab Assistant, Research Coordinator, Research Scholar, Postdoctoral Researcher, Graduate Research Assistant, Research Assistant Intern, Outpatient Pharmacy Intern, Clinical Affairs Intern, Clinical Fellow, Clinical Nurse, Clinical Operations Manager, Clinical Research Professional, Assistant Professor, Lecturer, Graduate Teaching Assistant, Clinical Research Manager, Pharmacy Operations Manager, Associate Director of Clinical Development, Vice President of Clinical Development, Drug Safety Associate, Regulatory Specialist, Scientific Consultant, Medical Laboratory Scientist, Pharmacovigilance Associate, NHS Primary Care QI Facilitator, Government Healthcare Recruiter, Research Ethics Coordinator.
"From International PV Roles To North American Market Success – the detailed modules prepared me excellently for real-world applications." – John Vinil
Companies: Novo Nordisk, Moderna, Abbott, Accenture, CVS, Walgreens, FDA, VA, GoodRx, Merck, NIH, MOH Ontario, Thermo Fisher Scientific, Procter & Gamble, AbbVie, Parexel, Regeneron, Bristol Myers Squibb, IQVIA, Memorial Sloan Kettering, NewYork-Presbyterian, Johns Hopkins, Tufts, Beth Israel Deaconess, UF Health Cancer Center, MD Anderson, Emory Healthcare, Eli Lilly, L'Oréal, Northwestern Medicine.
Job Roles: Regulatory Affairs Associate, Clinical Trial Drug Safety Associate, Drug Safety Specialist, Patient Safety Senior Associate, Pharmacovigilance Scientist, Pharmacovigilance Manager, Senior Pharmacovigilance Associate, Regional Head, Pharmacovigilance Analyst, Senior Director Quality, Data Entry Manager, Principal Pharmacovigilance Scientist, QA & Medical Complaint Handling Associate, Senior Manager Medical Safety Officer, Medical Affairs Senior Scientist, Quality Manager, VP Medical Affairs, Clinical Guidelines Coordinator, Clinical Data Monitor, Pharmacovigilance Specialist, Regulatory Project Manager, Product Safety Manager, Manager Pharmacovigilance Operations, Regulatory Affairs Manager, Clinical Pharmacist Consultant, Product Vigilance Manager, Epidemiologist, Senior Manager Safety and Pharmacovigilance, Associate Director of Pharmacovigilance, QPPV, Pharmacovigilance Deputy, Regulatory Affairs Supervisor, Senior Director Clinical Operations, Safety & Customer Service Excellence, QA Executive, Health Advisor, COVID Health Specialist, Senior Project Manager, Pharmacy Manager, R&D Post-Implementation Service, Investigations Associate, Lead Clinical Operations Safety/Quality Responsible.
"Promoted to Senior Startup Specialist in Clinical Trials – the course structure was very interactive and engaging." – Justin Scott Brathwaite
Companies: Moderna, Merck, IQVIA, ICON plc, Eli Lilly, AstraZeneca, VaxTrials, Deloitte, Procter & Gamble, Novotech, St. Jude Children's, Mount Sinai, U.S. DOH HHS, Mass General Hospital, HCA, Janssen Pharma, Tulane University, Memorial Sloan Kettering, Stanford University, University of Miami, University of Alberta, eClinicalWorks.
Job Roles: Clinical Research Associate, Clinical Trial Monitor II, Research Associate, CRA II, Scientist, Quality Assurance Analyst, Senior CRA, Research Associate in Discovery Immunology, Clinical Trial Monitor/CRA, Clinical Trials Project Manager, Associate Director of Research Nursing, Clinical Trial Navigator, Clinical Director for R&D, Medical Science Liaison, Clinical Trial Associate III, Quality Assurance Associate II, IRB/SRC Analyst II, Project Manager, Clinical Trial Associate, Clinical Research Coordinator, Public Health Advisor, Associate Scientist II, Strategy Analyst, Clinical Operations Specialist, Advisor - Development Clinical Research Scientist, Associate Clinical Engineer, Clinical Trial Management Associate, Quality Supervisor, Clinical Research Data Coordinator.
"From IMG to securing roles as a CRC, CRA, and now a project manager – joining this course was a pivotal step in my career advancement." – Dr. Vrushali Borawak
Companies: ION Pharmaceuticals, Teleflex, Baim Institute for Clinical Research, Aya Healthcare, Dermavant Sciences, Inventprise, iSTAR Medical, Oregon Health & Science University, Emory Office of Clinical Research, Flinders University.
Job Roles: Clinical Trial Project Manager, Research Nurse Manager, CRC-Data Manager, Clinical Research Associate, Transdisciplinary Research Project Manager, IT Project Manager in Clinical Research, Publicly Funded Research Project Manager.
"ICH GCP made me more confident in research – this course covered in depth beyond mere theory." – Aastha Shah
Companies: US Army Medical Research & Materiel Command, Yale School of Medicine, Oxford University Clinical Research Unit, Illumina, Merck Healthcare, IQVIA Canada, CDC Foundation, British Journal of Dermatology, UT MD Anderson, International Medical Corps.
Job Roles: Clinical Research Medical Monitor, Medical Monitor, Principal Medical Monitor, Lead Medical Monitor, Clinical Trial Medical Monitor, Medical Oversight Director, Associate Medical Monitor, Senior Medical Monitor, Clinical Study Physician, Medical Advisor for Clinical Research, Clinical Research Physician, Medical Safety Monitor, Medical Director of Clinical Research, Drug Safety Medical Monitor.
"From International PV Roles To North American Market Success – the modules prepared me excellently for real-world applications." – John Vinil
Companies: Accelemed Research, Zion Healthcare, CAP Research, Quotient Sciences, Profil Institut für Stoffwechselforschung GmbH, Physician Affiliate Group of New York, San Carlos Apache Healthcare Corporation, DBA Cairn Diagnostics, IMA Research Austin Group, Lucas Research.
Job Roles: Principal Investigator, Principal Research Investigator, Senior Principal Investigator, Clinical Trial Principal Investigator, Clinical Research Nurse Investigator, Oncology Principal Investigator, Radiation Therapy Principal Investigator, Academic Principal Investigator, Healthcare Settings Principal Investigator.
"The hands-on activities throughout the course solidified my understanding of complex concepts." – Umber Mahmood
Read how a dedicated IMG transformed into a successful Clinical Research Coordinator, leveraging our world-class training.
"The flexible online format allowed me to balance my studies with my professional commitments seamlessly." – Aishwarya Sukumar
Discover how our training enabled a transition to a leadership role in clinical research across international markets.
"I was able to immediately apply what I learned to my job." – Rose Hyson
See how our program prepared a candidate to successfully transition into clinical trials project management.
"The course was structured, interactive, and engaging from start to finish." – Justin Scott Brathwaite
Learn how our training propelled a professional into a senior leadership role in clinical trials.
"The materials were clear, well-organized, and directly applicable to my work." – Renata Noronha
See how our training prepared a candidate to excel as a safety associate in clinical research.
"The quality of delivery and materials was exceptional." – Ossai Opene
Read how an advanced degree transformed into a successful clinical research career.
"In-depth content and expert instructors provided invaluable insights." – Celia Moon
Discover how our program enabled a physical therapist to transition into clinical research.
"Joining this course was a pivotal step in my career advancement." – Dr. Vrushali Borawak
Learn how our training facilitated a career transformation from IMG to leadership roles in clinical research.
"The course went in depth, ensuring concepts were fully understood." – Aastha Shah
Explore how our ICH GCP training boosted a professional’s confidence and career prospects.
"I now feel more competent and confident in my role." – Stephanie
See how mastering ICH GCP has transformed a professional’s expertise in clinical research.
"The course helped me secure a role in regulatory affairs at a top clinical research site." – Scott Boyle
Discover the journey from intern to a successful Regulatory Affairs Associate in the North American market.
Our dedicated course advisor in the clinical research field is here to help you succeed. Schedule a career and course advising session today and receive personalized guidance to propel your clinical research career.
Grad Placements:
Grad Placements:
Grad Placements:
Grad Placements:
Grad Placements:
Grad Placements:
Grad Placements:
Grad Placements:
Choose the Right Clinical Research Program for Your Career
Flexible in-house payment plans available starting at just $500/month.
For entry-level professionals, academic researchers, and career changers
Master initiation visit readiness, subject documentation, and sponsor-required logs along with advanced GCP workflows. Alumni are thriving worldwide.
Starting at $1,299
• Initiation visit readiness
• Subject documentation
• Sponsor-required logs
• Advanced GCP workflows
• Mentors assigned at every level
For aspiring and current Clinical Research Coordinators
Lead full protocol execution and trial oversight by mastering AE/SAE documentation, protocol deviation management, and essential business skills. Our courses are dedicated to lifelong career success.
Starting at $1,499
• Advanced AE/SAE documentation
• Protocol deviation management
• PI-submission alignment
• Full visit lifecycle preparation
• Expert mentorship and 24/7 support
For experienced CRCs, CTAs, and nurses
Excel as a Clinical Research Associate by mastering advanced SDV, risk-based oversight, and effective communication strategies. Benefit from the largest curriculum update in 2025.
Starting at $1,599
• Monitoring visit excellence
• Complex deviation handling
• SDV auditing
• Communication strategies
• Live webinar support
For physicians and site leaders
Gain flexible PI training to master sponsor selection, trial specialties, and IRB compliance. Our program is dedicated to lifelong career success and includes a 100% money-back guarantee.
Starting at $1,499
• Sponsor-facing protocol review
• IRB compliance mastery
• Delegation & safety review processes
• Personalized coaching
For scientific professionals
Develop strategic skills in scientific engagement, KOL strategy, and therapeutic expertise. Our dedicated mentors and 24/7 support ensure your success in competitive MSL/MM roles.
Starting at $1,599
• Scientific engagement
• KOL strategy
• Therapeutic expertise
• Cross-department collaboration
• 24/7 support
For regulatory and safety professionals
Become a top regulatory strategist by mastering DSUR, PSUR, PBRER, and MedDRA-driven ICSR workflows. Our courses are CPD accredited and are dedicated to lifelong career success.
Starting at $1,499
• DSUR, PSUR, PBRER development
• MedDRA-driven ICSR workflows
• End-to-end regulatory documentation
• Expert-led strategy sessions
• 24/7 course support
For CRAs, CTMs, and project managers
Enhance your leadership skills with advanced project tracking, milestone forecasting, and cross-functional team management. Our alumni are thriving in leadership roles.
Starting at $1,599
• Advanced project tracking
• Milestone forecasting
• Cross-functional leadership
• Communication frameworks
• Dedicated mentor support
For professionals seeking applied ICH GCP training
Master advanced ICH GCP interpretation, regulatory binder preparation, and consent management to boost your documentation precision. Experience the largest curriculum update in 2025!
Starting at $999
• Advanced ICH GCP interpretation
• Regulatory binder preparation
• Consent management & site standardization
• Expert mentorship and career coaching
CCRPS (Certified Clinical Research Professionals Society) offers the most intensive clinical research training and certification available online. Our programs are designed to maximize your potential, improve job prospects, and accelerate career advancement in clinical research.
We provide certifications for Clinical Research Associate, Clinical Research Coordinator, Good Clinical Practice (CPD accredited), Medical Monitor, Pharmacovigilance Specialist, Clinical Project Manager, Research Assistant, and Principal Investigator—each tailored to elevate your clinical research training.
Yes, our courses are accredited by ACCRE, NHA, and CME providers including ANCC, ACCME, and ACPE through JA/PIMED. They meet global standards such as TransCelerate Biopharma, and our programs are CPD accredited.
Our self-paced programs are designed for completion in 1-4 weeks with rolling enrollment and live weekly exam reviews. Advanced modules can be skipped if they don't align with your career goals.
Each clinical research course includes over 600 updated modules featuring interactive lessons, videos, review tables, application assessments, study guides, and live exam review webinars. Every module includes practice questions to ensure thorough understanding.
Our training is perfect for beginners, recent graduates, experienced professionals, physicians, nurses, and industry experts. It is designed to maximize your potential as a researcher and is proven to enhance job prospects and promotion rates.
Yes, all enrolled students receive lifetime access to course materials, including regular updates (available until March 2025) to keep you current with industry standards.
Pricing starts at $999 and varies by program. We offer flexible payment options via Stripe, Affirm, Afterpay, and Klarna, as well as in-house payment plans starting at $500/month.
Yes, we provide one-on-one mentorship, resume assistance, and job placement support to help you secure a rewarding role in clinical research.
Absolutely. All our clinical research courses are 100% online and self-paced, with live instruction available every 1-4 weeks. Access them on desktop or mobile devices anytime.
If you have no clinical or healthcare background, we recommend our Research Assistant or Clinical Research Coordinator courses to build the foundational knowledge for entry-level roles.
For individuals with some clinical experience or a healthcare/science degree, our Clinical Research Coordinator or Clinical Research Associate courses refine your skills in trial management and monitoring.
If you have significant clinical or research experience, consider our Pharmacovigilance & Regulatory Affairs, Medical Monitor, Clinical Project Manager, or Principal Investigator courses to enhance your leadership and specialized skills.
CCRPS offers the most intensive online clinical research course available—backed by the largest curriculum update in 2025, dedicated mentor support at every level, 24/7 course support, and a 100% money-back guarantee. Our alumni are thriving globally.
CCRPS certifications provide comprehensive and advanced training for all experience levels. In contrast, ACRP and SOCRA credentials are geared toward professionals with at least two years of experience and include additional memberships and proctored exams. Our curriculum aligns with industry standards to support your exam success.
Simply visit our website, choose your desired clinical research program from our pricing grid, and enroll instantly. Start risk-free with our 100% money-back guarantee.
Graduates gain globally recognized credentials, enhanced skills, and access to a professional network of over 26,000 members. Many secure roles or promotions within six months of certification.
Our dedicated advisors are available 24/7. Contact us via SMS or call +1 (239) 329-9837, or chat with us on our website for personalized guidance.
Certified professionals often see salaries ranging from $60K to $160K+ per year, with faster promotions and increased job prospects thanks to our rigorous training.
Our graduates work at leading hospitals, research institutions, pharmaceutical companies, CROs, and government agencies such as Mayo Clinic, Johns Hopkins, NYU Langone, Pfizer, AstraZeneca, Merck, Novartis, IQVIA, Parexel, ICON, FDA, NIH, and CDC.
The demand for top-tier clinical research professionals is soaring globally. Our training ensures you have the expertise to drive medical advancements and excel in your career.
Certification opens diverse career opportunities, provides global recognition, accelerates career advancement, and helps you master critical areas such as GCP, decentralized trials, and regulatory compliance.
Our intensive, hands-on training, real-world case studies, and trial simulations improve your interview success, boost hiring rates, and accelerate promotions.
Yes, we offer group orders and staff/site training licenses at a flat rate of $5,000 per course.
CCRPS delivers an advanced curriculum, lifetime content access, dedicated mentor support, 24/7 course support, and a 100% money-back guarantee. Our training is the gold standard for clinical research courses—trusted by over 26,000 professionals worldwide for lifelong career success.
Join over 26,000 professionals who have transformed their careers with the best clinical research training in the world. Enroll now to unlock globally recognized credentials, cutting-edge training, and lifelong support.
Enroll TodayMaster and understand Good Clinical Practice with advanced GCP certification recognized by TransCelerate Biopharma. Updated for E6 R3 standards and includes a 25-question final exam with live weekly review.
Start and excel as a research assistant with ACCRE and CME-accredited certification. Gain expert-level skills in trial design and protocol development to advance your career.
Get the most advanced coordinator training accredited by ACCRE and CME. Master advanced CRC skills, specialties, medical devices, and global trials with comprehensive support.
The most comprehensive CRA training program accredited by ACCRE and CME. Build advanced CRA monitoring skills across various trial types and specialties with dedicated mentorship.
Receive leading advanced training in international pharmacovigilance and regulatory affairs accredited for CME. Covers advanced topics for multi-national trials with mentorship and recognized certification.
Master project management in clinical research with a program focused on advanced project management and research skills. Complete daily modules with expert mentorship and career support.
Physicians gain monitoring certification across diverse trial specialties and designs with our accredited program. Internationally recognized, this training empowers you with advanced monitoring skills.
Cutting-edge, flexible PI training with CME. Learn sponsor selection, trial specialties, and advanced PI skills with a curriculum tailored to your specialty, complete with a study guide and live review sessions.
Become part of the CCRPS WhatsApp Community—join over 26,000 researchers in our free clinical research network as we expand networking events and community resources.
Join Now