Clinical Research Certification By CCRPS
Advanced Clinical Research Training for All Levels
Triple-Accredited Online Clinical Research Courses for Career Excellence
Start or Advance with the #1 Most Comprehensive Triple-Accredited Clinical Research Courses with Alumni Working At 1,600+ Orgs.
Get CPD, CE, & ACCRE Accredited Clinical Research Certifications with NHA-Backed Partnership and 8 Years of Alumni Success.
Our Clinical Research Training Programs offer 70-288 Role-Specific Lessons Across Trial Specialties, Designs, Global Guidelines, Devices, and Expert-Skills.
Get Hired & Promoted with Next-Level Clinical Research Knowledge Gained Easily Through Interactive, Application-focused Lessons, 100s Cases, Toolkits, Videos, MCQs, Live Webinars & More.
Fast-Track Your Clinical Research Career with 1–4 Week Bootcamps or 3–6 Month Self-Paced Track. Gain PDF + URL Certificate and LinkedIn Badge Used by 1,900 Researchers.
Enroll Now or Chat/Call +1 (239) 329‑9837 I 14 Day Refund Policy & Flexible Payment Plans I Request Employer Reimbursement for Training
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Advanced Clinical Research Coordinator Certification (ACRCC)
Objective: Equip participants with end‑to‑end expertise in clinical trial coordination; from protocol interpretation, regulatory submissions, and informed consent through site activation, data and safety monitoring, risk‑based quality control, patient recruitment, budget and supply management, and decentralized trial integration to leadership and ethical cultural competency to ensure patient safety, data integrity, and regulatory compliance throughout the trial lifecycle.
Prerequisites: High school diploma or GED OR current nurse OR professional with patient‑care experience.
Format & Length: Led by expert CRCs Morgan Hess & Breanna Throne. Advanced, online, self‑paced; 110 CPD hours over 4–12 weeks; start anytime.
Accreditation: CPD‑accredited; ACCRE; Joint Accreditation with ANCC for 17.5 CME (nurses).
Certification Requirements: ≥ 70% on final exam (up to two attempts); online certificate awarded upon passing.
Graduates work at: Pharmaceutical and Biotech Companies, Hospitals and Healthcare Providers, Universities and Academic Institutions, Clinical Research and Consulting Services, Diagnostic Services, Consumer Goods Companies, Healthcare Services, Cancer Treatment and Research Centers.
Graduates Hired As: Clinical Research Coordinator I & II, Lead/Senior CRC, Oncology Research Coordinator, Clinical Study Coordinator, Clinical Research Data Coordinator, Clinical Research Nurse, Clinical Director/Office Manager, Regulatory Contact/CRC, Clinical Research/Regulatory Coordinator, Clinical Trials Specialist, Research Regulatory Specialist, Certified Clinical Research Coordinator, Clinical Research Specialist, Sr. Director of Clinical Operations.
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Advanced Clinical Research Associate Certification (ACRAC)
Objective: Equip participants with end‑to‑end expertise in clinical research associate functions; from protocol analysis and regulatory submission preparation, through on‑site and remote monitoring visits, source document verification, query resolution, vendor and site relationship management, safety reporting, and risk‑based monitoring, to data management, project coordination, decentralized trial methodologies, and cross‑functional communication to ensure site compliance, patient safety, and data integrity across all phases of clinical trials.
Prerequisites: Bachelor’s in Biology/Natural Science, Nursing degree, or MBBS/IMG for entry‑level; consideration for major industry credentials after ≥ 2 years’ experience; 18% of participants already credentialed/experienced use the course for a comprehensive knowledge refresh.
Format & Length: Led by expert CRAs Dr.Gill & Dr.Albano. Advanced, online, self‑paced; 290 hours total; start anytime. Finish in 4-16 weeks.
Accreditation: 290 CPD hours; ACCRE; Joint Accreditation for CE with ACCME, ANCC, ACPE & ICPE (17.5 CME for physicians, nurses, pharmacists & healthcare professionals).
Certification Requirements: ≥ 70% on final exam (up to two attempts); online certificate awarded upon passing.
Graduates Work At: Pharmaceutical & biotech companies; clinical research & consulting services; consulting & professional services; consumer goods companies; hospitals & healthcare providers; government health departments; universities & academic institutions; healthcare IT & services.
Graduate Job Roles Landed: Clinical Research Associate; Clinical Trial Monitor II; Research Associate; CRA II; Scientist; Quality Assurance Analyst; Senior Clinical Research Associate; 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; Clinical Research Professional; 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, Neuroscience; Associate Clinical Engineer; Clinical Trial Management Associate; Quality Supervisor; Clinical Research Data Coordinator.
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Advanced Pharmacovigilance and Regulatory Affairs Certification (APRAC)
Objective: Equip participants with comprehensive proficiency in global pharmacovigilance, from interpreting ICH, FDA, EMA, and CIOMS regulations; through end‑to‑end case management in Oracle Argus; adverse event and SAE reporting; signal detection, risk management, and quality systems; safety database configuration and KPI monitoring; aggregate report compilation and labeling updates; cross‑functional collaboration; specialized PV operations for biologics, vaccines, and devices; to regulatory submission support to ensure drug safety, compliance, and data integrity across all pharmacovigilance activities.
Prerequisites: Bachelor’s in Biology or Natural Science OR Pharmacist degree; Prior clinical research experience or advanced medical degree required.
Format & Length: Led by expert PV specialists Vinil John and Dr.Bilal, MBBS, Phd. Advanced, online, self‑paced; 180 hours; start anytime.
Accreditation: 180 CPD hours; ACCRE; Joint Accreditation for CE with ACPE (17.5 CME for pharmacists). Finish in 3-14 weeks.
Certification Requirements: ≥ 70% on final exam (up to two attempts); online certificate awarded upon passing.
Graduates Work At: Pharmaceutical & biotech companies; healthcare service providers; regulatory bodies & research institutes; consulting & services firms; consumer goods companies; healthcare information & services organizations.
Graduate Hired As: Regulatory Affairs Associate, Clinical Trial Drug Safety Associate, Drug Safety Specialist, Patient Safety Senior Associate, Pharmacovigilance Scientist, Pharmacovigilance Manager, Senior Pharmacovigilance Associate, Pharmacovigilance Regional Head, Pharmacovigilance Analyst, Senior Director Quality, Pharmacovigilance 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 Department, Qualified Person Responsible for Pharmacovigilance (QPPV), Pharmacovigilance Deputy, Senior Scientist, Senior Medical Advisor, Cosmetovigilance Specialist, Drug Safety and Medical Information Specialist, Environmental Analyst, Vice President Clinical Development, Operations Specialist (Life Cycle Safety/Drug Safety/Medical Information), Regulatory Affairs Supervisor, Senior Director Clinical Operations Safety and Customer Service Excellence, Regulatory Affairs – Pharmacist, Vice President Operations, QA Executive, Health Advisor Pharmacist, COVID Health Specialist – Case and Contact Manager, Senior Project Manager, Pharmacy Manager, R&D Post‑Implementation Service Lead, Investigations Associate, Lead Clinical Operations Safety/Quality Responsible, Pharmacist Trial and Supply Management
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Advanced Clinical Research Project Manager Certification (ACRPMC)
Objective: Equip participants with end‑to‑end expertise in managing multi‑center clinical trials, from protocol development and study budgeting; through resource allocation, vendor & stakeholder management, site feasibility, activation, and risk‑based quality control; supply chain and logistics oversight; timeline management and project tracking; to leadership, cross‑functional communication, regulatory compliance, and project close‑out; to ensure on‑time, on‑budget, and compliant delivery of large‑scale clinical research.
Enrollment: 1,352 students from CROs, universities, hospitals, and clinics.
Prerequisites: Prior project management or clinical research experience.
Format & Length: Led by Inci Gunes. Advanced, online, self‑paced; 290 hours delivered across 290 lessons; start anytime. Finish in 4-16 weeks.
Accreditation: 290 CPD hours; ACCRE; Joint Accreditation for CME.
Certification Requirements: ≥ 70% on final exam (up to two attempts); online certificate awarded upon passing.
Graduates work at: Pharmaceutical & biotech companies; clinical research & consulting services; healthcare staffing; universities & academic institutions.
Graduate Job Roles: Clinical Trial Project Manager, Research Nurse Manager, Clinical Research Coordinator‑Data Manager, Clinical Research Associate, Transdisciplinary Research Project Manager, IT Project Manager in Clinical Research, Publicly Funded Research Project Manager.
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Advanced Dual Medical Science Liaison & Monitor Certification (AMSLC)
Objective: Equip physician participants with end‑to‑end expertise in medical monitoring and field medical liaison functions; from in‑depth protocol review, safety strategy development, and DSMB support; through adverse event medical review, causality assessment, and aggregate safety reporting; to data interpretation, statistical overview, cross‑functional communication with clinical operations and regulatory affairs, publication planning, and investigator engagement, to ensure patient safety, scientific rigor, and regulatory compliance across the trial lifecycle.
Enrollment: 1,962 physicians from pharmaceutical & biotech companies, CROs, academic medical centers, and healthcare providers.
Prerequisites: Advanced Medical Degree (PhD in Pharm/Bio, PharmD, MD, MBBS, IMG, FMG).
Format & Length: Led by MM Anas & Expert MSL, Dr.Albano. Advanced, online, self‑paced; 250 hours delivered across 240 + lessons; start anytime.
Accreditation: 250 CPD hours; Joint Accreditation with the AMA for 17.5 CME.
Certification Requirements: ≥ 70% on final exam (up to two attempts); online certificate awarded upon passing.
Graduates Work At: Pharmaceutical & biotech companies, contract research organizations (CROs), academic research institutions & medical schools, government health agencies & public health foundations, clinical trials units & research hospitals, medical affairs consultancies & scientific journals, healthcare technology & data analytics firms.
Graduate 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.
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Advanced Research Principal Investigator Certification (ARPIC)
Objective: Built on real‑world mentorship and interactive case studies, this program guides licensed physicians through every stage of the PI role, understanding study design and endpoint selection, crafting robust informed consent strategies, navigating regulatory submissions, supervising site performance, interpreting safety and efficacy data, empowering study teams through effective delegation and communication, and fostering ethical, patient‑centric research to develop confident, collaborative leaders who drive high quality clinical trials.
Enrollment: Physicians and SubIs from diverse backgrounds, including academic medical centers, hospital research units, biotech and pharma sponsors, government health agencies, and independent clinical research sites.
Prerequisites: Active medical degree; non‑active MDs, PhDs, and PharmDs qualify for Sub‑Investigator positions.
Format & Length: Led by Dr.Martella. Advanced, online, self‑paced; 179 CPD hours across 170+ lessons; start anytime. Finish in 2-16 weeks (accelerated).
Accreditation: 179 CPD hours; Joint Accreditation with the AMA for 17.5 CME credits.
Certification Requirements: ≥ 70% on final exam (two attempts max); online certificate awarded upon passing.
Graduates Work At: Biotech & pharmaceutical companies, academic research institutions, government & regulatory agencies, non‑profit research consortia, hospital‑based clinical research centers, global CROs, and healthcare technology firms.
Graduate Job Roles: Principal Investigator, Sub‑Investigator, Clinical Research Director, Study Physician, Clinical Trial Lead, Medical Science Liaison (Investigator Relations), Clinical Research Consultant, Safety Medical Monitor, Ethics Committee Member, Investigator Site Manager, Clinical Operations Physician, Research Quality Lead.
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Advanced Clinical Research Assistant Certification (ACTAC)
Objective: Provide participants with in‑depth skills to support all aspects of clinical trial operations—from study start‑up logistics, regulatory document preparation, and informed consent coordination; through source document management, eCRF data entry, query resolution, patient scheduling, and safety‑reporting assistance; to quality control, vendor coordination, and effective cross‑functional collaboration to ensure efficient, compliant, and patient‑centric trial support.
Prerequisites: High school diploma or GED, or bachelor’s degree in life sciences or allied health, or prior healthcare/clinical support experience.
Format & Length: Led by former RA, Ahmad Mohamad. Advanced, online, self‑paced; 110+ CPD hour across 114 lessons; start anytime. Avg. 3-12 Weeks.
Accreditation: 114 CPD Hours, ACCRE; Joint Accreditation for CME.
Certification Requirements: ≥ 70% on final exam (up to two attempts); online certificate awarded upon passing.
Students Came From: Various CROs, universities, hospitals, clinics, and clinical research sites.
Graduates Work At: Pharmaceutical & biotech companies, hospitals & healthcare providers, CROs, academic research institutions, government health agencies, clinical laboratories.
Graduate Job Roles: Clinical Research Assistant, Study Coordinator Assistant, Clinical Trial Documentation Specialist, eCRF Data Coordinator, Regulatory Documentation Clerk, Patient Recruitment Coordinator, Site File Manager, Clinical Trial Scheduler, Informed Consent Specialist, Quality Assurance Assistant, Research Data Entry Specialist, Patient Screening Specialist, Trial Master File Coordinator, Site Liaison, Clinical Office Administrator.
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Advanced ICH Good Clinical Practice Certification (AGCPC)
Objective: Equip clinical research professionals with a thorough understanding of ICH E6(R3) GCP principles, ethical compliance, informed consent processes, data integrity standards, monitoring requirements, and regulatory obligations to ensure global trial quality and participant safety.
Enrollment: Open enrollment for research professionals across academia, healthcare institutions, regulatory bodies, and industry.
Prerequisites: None; recommended for all personnel involved in clinical research.
Format & Length: Led by expert research writer, Dr.Cliff Dominy, PhD. Advanced, online, self‑paced; 70 lessons,, finish in 1-4 weeks.
Accreditation: CPD‑accredited 70 CPD hours.
Certification Requirements: ≥ 70% on final exam; online certificate awarded upon passing.
Graduates Work At: 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 Health, Anderson, Colorado State University, Baylor, Kaiser, Cornell, Boston University.
Graduate 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.
See Where CCRPS Alumni Work
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Graduates work at: 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, etc.
Graduate job roles post-course: Clinical Research Coordinator, Clinical Research Coordinator II, Lead Clinical Research Coordinator, Senior Clinical Research Coordinator, Oncology Research Coordinator, Clinical Study Coordinator, Clinical Research Data Coordinator, Clinical Research Nurse, Clinical Director/ Office Manager, Regulatory Contact/ Clinical Research Coordinator, Clinical Research/Regulatory Coordinator, Clinical Trials Specialist, Research Regulatory Specialist, Certified Clinical Research Coordinator, Clinical Research Specialist, Sr. Director of Clinical Operations (based on review of new job positions post-enrollment)
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Graduates work at: Moderna, Merck, IQVIA, ICON plc, Eli Lilly and Company, AstraZeneca, VaxTrials, Deloitte, Procter & Gamble, Novotech, St Jude Children's, Mount Sinai, U.S. DOH HHS, Mass General Hospital, HCA Hospital, Janssen Pharma (J&J), Tulane University, Memorial Sloan Kettering Cancer Center, Stanford University, University of Miami, VaxTrials, Deloitte, Procter & Gamble, Novotech, University of Alberta, eClinicalWorks, etc. ‡
Graduate job roles post-course: Clinical Research Associate, Clinical Trial Monitor II, Research Associate, CRA II, Scientist, Quality Assurance Analyst, Senior Clinical Research Associate, 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, Senior Clinical Research Associate, Clinical Research Professional, 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 Research Associate II, Clinical Operations Specialist, Advisor - Development Clinical Research Scientist, Neuroscience, Associate Clinical Engineer, Clinical Trial Management Associate, Quality Supervisor, Clinical Research Data Coordinator (based on review of new job positions post-enrollment)
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Graduates work at: 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, CVS, Memorial Sloan Kettering Cancer Center, NewYork-Presbyterian Hospital,Johns Hopkins Medicine, Tufts Medical Center, Beth Israel Deaconess Medical Center, UF Health Cancer Center, MD Anderson Cancer Center, Emory Healthcare, Eli Lilly and Company, L'Oréal, Northwestern Medicine, etc‡
Graduate Hired As: Regulatory Affairs Associate, Clinical Trial Drug Safety Associate, Drug Safety Specialist, Patient Safety Senior Associate, Pharmacovigilance Scientist, Pharmacovigilance Manager, Senior Pharmacovigilance Associate, Pharmacovigilance Regional Head, Pharmacovigilance Analyst, Senior Director Quality, Pharmacovigilance 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 Department, Qualified Person Responsible for Pharmacovigilance (QPPV), Pharmacovigilance Deputy, Regulatory Affairs Manager, Senior Scientist, Senior Medical Advisor, Cosmetovigilance, Drug Safety and Medical Information Specialist, Environmental Analyst, Vice President Clinical Development, Operation Specialist (Life Cycle Safety/Drug Safety/Medical Information), Regulatory Affairs Supervisor & QPPV, Senior Director Clinical Operations, Safety, and Customer Service Excellence, Regulatory Affairs - Pharmacist, Vice President Operations, QA Executive, Health Advisor Pharmacist, COVID Health Specialist - Case and Contact Manager, Senior Project Manager, Pharmacy Manager, R&D Post-Implementation Service, Pharmacy Manager, Investigations Associate, Lead Clinical Operations Safety/Quality Responsible, Pharmacist, Trial and Supply Management, etc. (based on review of new job positions post-enrollment)
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Students came from various CROs, universities, hospitals, clinics, and clinical research sites, etc.‡
Graduates work at: ION Pharmaceuticals, Inc., Teleflex, Baim Institute for Clinical Research, Aya Healthcare, Dermavant Sciences, Inventprise, iSTAR Medical, Oregon Health & Science University, Emory Office of Clinical Research, Flinders University, etc.
Graduates obtained roles including: Clinical Trial Project Manager, Research Nurse Manager, Clinical Research Coordinator- Data Manager, Clinical Research Associate, Transdisciplinary Research Project Manager, IT Project Manager in Clinical Research, Publicly Funded Research Project Manager.
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Graduates worked at US Army Medical Research and Materiel Command, Yale School of Medicine (YCCI), Oxford University Clinical Research Unit, Illumina, Merck Healthcare, IQVIA Canada, CDC Foundation, British Journal of Dermatology, UT MD Anderson Cancer Center, International Medical Corps, etc, etc.‡
Graduates obtained roles including: Clinical Research Medical Monitor, Medical Science Liaison, 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
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Graduates worked at various CROs, universities, hospitals, clinics, and clinical research sites, etc.
Graduates obtained roles including: Principal Investigator in Clinical Research, Principal Research Investigator, Senior PI, Clinical Trial PI, and more
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Graduates worked at: Various universities, hospitals, clinics, scholarships, internships, and clinical research sites.
Graduate job roles post-course: Clinical research assistant, clinical trial assistant, clinical researcher professional, clinical research coordinator, trial assistant, research assistant.
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Graduates work at: University research groups, hospitals, clinics, clinical trial sites, pharmaceutical companies, and government agencies i.e. FDA, NHS, ICON PLC, PPD, IQVIA, Parexel, Johnson & Johnson, Medtronic, Novartis, Novo Nordisk, UNC Health, NYU Langone Health, Anderson, Colorado State University, Baylor, Kaiser, Cornell, Boston University, ‡
Graduate Job Roles after course: ICH GCP training is required every 2 years for all research roles thus our graduates work in a range of fields. Research roles: Research Assistant, Lab Assistant, Research Coordinator, Research Scholar, Postdoctoral Researcher, Graduate Research Assistant, etc. Intern roles: Research Assistant Intern, Outpatient Pharmacy Intern, Clinical roles: Clinical Affairs Intern, Clinical Fellow, Clinical Nurse, Clinical Operations Manager, Clinical Research Professional Teaching roles: Assistant Professor, Lecturer, Graduate Teaching Assistant, etc. Management roles: Clinical Research Manager, Pharmacy Operations Manager, Associate Director of Clinical Development, Vice President of Clinical Development Specialized roles: Drug Safety Associate, Regulatory Specialist, Scientific Consultant, Medical Laboratory Scientist, Pharmacovigilance Associate Other roles: NHS Primary Care QI Facilitator, Government Healthcare Recruiter, Research Ethics Coordinator (based on review of new job positions after enrollment in course)
Clinical Research Careers Begin & Advance Here.
Upcoming Job Board & Career Center: Exclusive to all 8 programs (thanks to our VP Careers, Mehwish)
10K+ Alumni Network: Placed at 1,600+ employers worldwide
Weekly Community Events: Live webinars, expert panels, peer discussions; share wins on LinkedIn & tap into our 1K+ growing CR WhatsApp group
Fast‑Track Outcomes: 23% of graduates in managerial roles; 1 in 4 students already hold credentials or 2+ years experience but choose to add CCRPS to bridge knowledge gaps
Career Switch Support: Nurses→CRCs, scientists→CRAs, PMPs/Mid-Level Researchers→Managers, PhDs/MDs-> PIs & MSLs, PharmDs -> PV/RA, and more (career quiz)
Ongoing Services: Practice exams, case simulations, career accelerator programs (175 lessons for internship to leadership for each course), mock interviews, mentorship, 1-1 job and internship placement support, educational internship (only 3 per quarter). ,
Explore Our Leading Clinical Research Courses
Become industry‑ready with our leading Advanced Clinical Research Training Courses & Certification in weeks, not years. If you're tired of being overlooked, our novel intensive certificate training programs are designed to get you job-fluent & hired. Demo our unmatched curriculum and see why alumni choose CCRPS for career training. .
Accreditations & Partners
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CCRPS is officially CPD-accredited for all eight of its clinical research certification programs, with each clinical research course offering 70 to 295 CPD hours, depending on the curriculum depth. CPD Standards Office (CPDSO) CCRPS is proud to be an accredited provider with the Continuing Professional Development Standards Office (CPDSO), a globally recognized organization supporting professional education and lifelong learning. Our Clinical Research Associate Certification has undergone a rigorous evaluation and has been awarded CPD accreditation, confirming that the course meets the highest standards for content, structure, and educational quality. As part of this accreditation, CCRPS is authorized to issue CPD Certificates of Completion to delegates who successfully complete the course. Each certificate includes the total number of CPD hours earned and provides a Learning Reflection Tool to support compliance with international CPD schemes and professional body requirements. This CPD designation reflects our continued commitment to professional development and offers our students credentials recognized across multiple sectors, industries, and countries. CPDSO Provider Number: 50670 Our CPD-accredited courses support:
Lifelong learning and continuing education
Professional license renewals and skill development
Verified certificates indicating completed CPD hours
Our 8 CPD-Accredited Courses:
Clinical Research Coordinator Training - 110 CPD Hours
Clinical Research Associate (CRA) Training - 290 CPD Hours
Pharmacovigilance Training - 170 CPD Hours
Clinical Trials Assistant Training - 114 CPD Hours
Clinical Project Manager Training - 290 CPD Hours
Medical Monitor & MSL Training - 250 Hours
Principal Investigator (PI) Training - 179 Hours
ICH GCP Training - 70 Hours
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CCRPS’s CRA and CRC certification programs are accredited by the Accreditation Council for Clinical Research Education (ACCRE) since June 2019.
Accreditation Code: 463-03-005-GPC08This longstanding accreditation ensures:
Compliance with national professional standards
Industry recognition across biotech and pharmaceutical sectors
Continual evaluation for quality assurance and curriculum alignment
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Joint Accreditation – CME for Healthcare Professionals
CCRPS is Jointly Accredited through PIMED to offer Continuing Medical Education (CME) for physicians (ACCME/AMA), nurses (ANCC), pharmacists (ACPE), and more.
Advanced Clinical Research Professionals Course
Jointly Provided By: Postgraduate Institute for Medicine (PIM) & CCRPS
Release Date: July 14, 2020
Expiration Date: September 8, 2025
Estimated Time: 17.5 hours
Activity Code: 15592Target Audience: Clinical professionals in trial oversight and patient care.
Learning Objectives: Interpret ICH GCP protocols, explain quality monitoring, identify roles in audit/inspection, detect/report misconduct, and demonstrate competency via examination.Pharmacists: Credit is reported to CPE Monitor upon completion. Check your NABP account within 30 days.
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CCRPS is a recognized partner institution of the NHA (Account #: 411862). Our Essentials of Leadership and Management in Health Care program supports professionals in advancing into leadership roles, preparing for NHA certification exams, and applying real-world management practices.
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CCRPS has been granted a state exemption under CRS 23-64-104, 1(h) for vocational education offered by a bona fide trade or professional organization. This allows us to focus on high-quality clinical research training without annual compliance reporting.
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CCRPS provides staff training for several small to mid-size CROs and sites. Our collaborative partnerships allow for site staff to engage in interactive training that researchers enjoy while improving compliance, efficiency, and outcomes for sites and CROs.
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CCRPS has partnered with the largest career board to provide free access to job listings for our alumni and community in June.
Trusted Gold-Standard Clinical Research Training For Career Advancement
Unmatched Training Curriculum for 2025 With New CPD Accreditation For Professional Growth
8 Years of Alumni Success. Grads At 1,600+ Organizations.
Accredited by CPD, ACCRE & Joint CE/CME. Aligned to ICH E6(R3), FDA, GVP, EMA GCP, and major guidelines.
Developed and updated by a global Scientific Advisory Board (Principal Dr.Rizvi) & Expert Panel.
Covers specialty trials, risk‑based monitoring, decentralized trial models, safety reporting, regulatory updates, and beyond for lifelong career success.
Interactive, self‑paced modules with live reviews, case simulations & practical exercises.
24/7 learner support via chat, mentors & peer forums + lifetime access to all materials and updates.
Chat with our dedicated team below.
CCRPS Case Studies
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From IMG to Clinical Research Coordinator at Columbia University: "This course not only met but exceeded my expectations with its thorough curriculum and insightful modules." -Lisa-Pierre
From IMG to Clinical Research Coordinator "The hands-on activities integrated throughout the course really helped solidify my understanding of complex concepts." -Umber Mahmood
From Physical Therapist to Clinical Researcher: "The in-depth content and expert instructors provided me with invaluable insights into the field." - Celia Moon
From International CRC to U.S. Lead CRC and CRA: "The flexible online format allowed me to balance my studies with my professional commitments seamlessly." - Aishwarya Sukumar
Enjoyed Clinical Research Training through Examples "The real-world examples used throughout the course were incredibly useful for applying theory to practice." -Marta Marszalek
Promoted to Senior Startup Specialist in Clinical Trials: "I appreciate how the course was structured—very interactive and engaging from start to finish." -Justin Scott Brathwaite
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From Clinical Research Receptionist to Certified Study Coordinator with CCRPS: "I highly recommend this course for its comprehensive approach and practical applications." - Katie Decker
Learning to Lead Safety Associate: "The course materials were clear, well-organized, and directly applicable to my work." - Renata Noronha
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
From Physician to Confident Drug Safety Specialist: "The course provided a robust foundation in the field, which was critical for my professional development." -Rabiea Bilal
From plant biologist to clinical recruitment administrative coordinator: "This program is a gateway to extensive knowledge and skills in a supportive learning environment." -Olajumoke Owati
ICH GCP Expert: "Thanks to this course, I feel more competent and confident in my role." - Stephanie
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From International PV Roles To North American Market Success: "The detailed modules prepared me excellently for real-world applications." - John Vinil
From Educational Research to Clinical Trials Project Management: "I was able to immediately apply what I learned in the course to my job." - Rose Hyson
From Coordinator to Clinical Research Grant Manager: "it really did a great job of the full scope of clinical research from start to finish." -Hannah Fischer
ICH GCP made her more confident in research: "this course just overall did a really good job going in depth, which I feel like wasn't just, it wasn't just covered just for the sake of covering content" - Aastha Shah
From Clinical Research Intern to Regulatory Affairs Associate at UPenn: "I would say since then. I've completed this course. It's helped me get my job in regulatory affairs at a clinical research site." - Scott Boyle
From Masters in Health Safety to Clinical Researcher: " I will say quality of delivery, quality of the materials. - Ossai Opene
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Proven Clinical Research Career Success Backed By Data & Interviews.
New and current clinical researchers train with CCRPS due to our intensive and comprehensive program.
Our syllabi for each of our 8 detailed programs speaks for itself.
See how we train you across specialties and keep you up to date with lifetime access with our all-inclusive clinical research training and certification programs.
Why Choose Our Online Clinical Research Training?
Train With the Clinical Research Course That Employers Know Is Advanced.
Master clinical trials, protocols, and ICH GCP E6 R3 standards.
When your resume says CCRPS, it says more than “completed a course.”
It says you're trained to the standards of top companies and 1,200+ clinical research organizations hiring right now.
Whether you’re aiming to lead as a Clinical Research Associate, pivot into Clinical Project Management, or formalize your experience with a CRC Clinical Research Certification, you’re backed by one of the most trusted clinical research training providers in the world.
âś“ Advanced Clinical Research Certifications created and taught by real-world Clinical Research Instructors and Certified experts. Trusted by alumni from 308 universities, 7 government agencies and 1200 organizations.
âś“ Fast track your certification in training in as little as 4 - 12 weeks and easily secure managerial or higher-level roles
âś“ Get a LinkedIn Badge for each Certificate in Clinical Research.
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“The flexible online format allowed me to balance my studies with my professional commitments seamlessly.”
— Aishwarya Sukumar, From International CRC to U.S. Lead CRC & CRA,
CCRPS Alumni
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“I appreciate how the course was structured — very interactive and engaging from start to finish.”
— Justin Brathwaite, Promoted to Senior Startup Specialist in Clinical Trials,
CCRPS Alum
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“CCRPS has a complete, really good approach. That’s what we offer to our sponsors — quality and safety, because we are all physicians.”
— Maria Lopez, Chief Medical Officer, CRA Program Partner,
CCRPS Alum
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“This course just did a really good job going in-depth... it wasn’t just content for content’s sake.”
— Aastha Shah, GCP Graduate,
CCRPS Alum
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“I highly recommend this course for its comprehensive approach and practical applications.”
— Katie Decker, From Receptionist to Certified Study Coordinator,
CCRPS Alum
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“I’ve completed this course. It helped me get my job in regulatory affairs at a clinical research site.”
— Scott Boyle, From Intern to Regulatory Affairs Associate, UPenn,
CCRPS Alum
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“The course materials were clear, well-organized, and directly applicable to my work.”
— Renata Noronha, From Learner to Safety Associate,
CCRPS Alum
Our Leading Accredited Clinical Research Certification Programs
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Good Clinical Practice Certification - GCP Clinical Research Certificate
Stay compliant with the latest ICH GCP E6 (R3) guidelines — required for all clinical researchers every 2 years. Designed for entry-level staff, students, and seasoned professionals needing renewal.
Duration: 1–4 weeks | 70 lessons | Live review with Dr. Cliff Dominy
Accredited by: CPD
Career Potential: $43,000–$76,000/year
Graduates work at: FDA, NIH, CROs -
CRA Training for Clinical Research
What should we know about the services you provide? Better descriptions result in more sales.
Get a top-tier Clinical Research Associate Certification with expertise in sponsor-site coordination, monitoring styles, and trial oversight.
Duration: 4–12 weeks | 288 lessons | Live mentorship + exam prep
Accredited by: ACCRE, CME (AMA, ANCC, ACPE)
Career Potential: $65,000–$103,000/year
Graduates work at: Moderna, IQVIA, Stanford, AstraZeneca -
(CRC) Clinical Research Coordinator Certification
Master trial site operations, data collection, and patient coordination with 20+ specialty tracks. Clinical Research Coordinator Certification is ideal for healthcare workers and entry-level professionals.
Duration: 4–8 weeks | 114 lessons | Instructor-led
Accredited by: ACCRE, CME (ANCC for nurses)
Career Potential: $59,000–$80,000/year
Graduates work at: Mayo Clinic, Cedars-Sinai, NYU Langone -
Pharmacovigilance Certification
Train in adverse event reporting, safety monitoring, and compliance across global regulations. Ideal for mid-level researchers and regulatory affairs professionals.
Duration: 4–8 weeks | 169 lessons | Real-world case studies
Accredited by: CME (ACPE for pharmacists)
Career Potential: $80,000–$120,000/year
Graduates work at: Moderna, Regeneron, Johns Hopkins -
Clinical Project Manager Certification
Transition from clinical staff to leadership in project management with a comprehensive curriculum tailored for CRAs, CRCs, and experienced researchers.
Duration: 4–12 weeks | 284 lessons | Leadership-focused
Accredited by: ACCRE, CME (AMA, ANCC, ACPE)
Career Potential: $80,000–$160,000/year
Graduates work as: Clinical PM, Data Manager, Research Nurse Manager -
Medical Science Liaison & Medical Monitor Certification
Build a career in clinical leadership, oversight, and regulatory management. Designed for physicians, PhDs, and international MDs.
Duration: 4–12 weeks | 249 lessons | Mentorship included
Accredited by: ACCRE, CME (AMA, ACPE)
Career Potential: $110,000+/year
Graduates work as: MSL, Medical Director, Medical Monitor -
Principal Investigator (PI) Certification
Designed for medical doctors and Sub‑Is. Lead trials as a Principal Investigator in global research and clinical settings.
Duration: 2–4 weeks | 171 lessons | Led by Dr. Martella
Accredited by: ACCRE, CME (AMA, ANCC, ACPE)
Career Potential: $150,000+ annually
Graduates work as: PI, Oncology PI, Research Director -
Clinical Research Assistant Training Program
Get started in clinical trials with a foundational role supporting data collection, documentation, and protocol execution.
HS/GED Required. Perfect for Premeds or Transitioning To Clinical Trials.
Duration: 3 Weeks | 115 Lessons | Interactive case studies | Instructor-led prep
Accredited by: ACCRE & CME
Career Potential: $42,000–$65,000/year
Graduates work as: Research Assistant, Trial Support Specialist, Clinical Data Technician
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