CCRPS


CCRPS is a global leader in clinical research education, offering advanced, accredited training programs designed to empower professionals to excel in clinical research careers. With a mission to provide accessible, high-quality education, CCRPS delivers comprehensive courses recognized by industry standards such as CPD, CME, and ACCRE, and has a proven track record of graduate success across 81 countries. The organization emphasizes innovation, integrity, and community building, supporting career advancement through expert-led instruction, real-world case studies, and extensive professional development resources.

Industries

clinical-trials
e-learning
pharmaceutical

Nr. of Employees

small (1-50)


Products

Clinical Research Associate (CRA) certification course

Advanced certification covering monitoring practices, protocol analysis, monitoring visit types, source verification, remote monitoring, and regulatory oversight for CRA roles.

Clinical Research Coordinator (CRC) certification course

Training focused on site operations, patient coordination, informed consent, data collection, and site management for CRC roles.

Pharmacovigilance and regulatory affairs certification

Curriculum on global pharmacovigilance regulations, case management, signal detection, aggregate reporting, and regulatory submission support for drug safety roles.

Clinical Project Manager certification

Program covering study budgeting, resource allocation, vendor management, supply chain, timeline tracking, and leadership skills for managing multi‑center trials.

ICH Good Clinical Practice (GCP) certification

Course focused on ICH GCP principles, trial ethics, data integrity, and regulatory obligations updated for E6(R3) and related ICH guidance.

Principal Investigator (PI) training course

Physician‑focused training covering PI roles, protocol oversight, safety reporting, informed consent, IND responsibilities, and site oversight checklists.

View All Products

Services

Role‑specific, self‑paced and instructor‑led online certification programs covering CRC, CRA, pharmacovigilance, PI, medical monitoring/MSL, project management, and ICH GCP with CPD/CME accreditation.

Customizable corporate training for CROs and research sites with SCORM compliance, branded portals/subdomains, PO billing, employee progress tracking, configurable module requirements, and immediate certificate issuance.

Annual or on‑demand ICH GCP refresher access for training departments to meet regulatory training requirements and support mutual recognition across sponsors.

Job board access, mock interviews, mentorship, internship placement, and career accelerator resources to support graduate hiring and promotion.

Expertise Areas

  • Clinical trial management
  • Monitoring and quality assurance
  • Pharmacovigilance and drug safety
  • ICH GCP and regulatory compliance
  • Show More (6)

Key Technologies

  • ICH GCP E6(R3) guidelines
  • Electronic data capture (EDC) / eCRF
  • Clinical Trial Management Systems (CTMS)
  • Safety case management systems / ICSR reporting
  • Show More (6)

News & Updates

A global online event for professionals to connect, share insights, and discuss industry trends.

An industry event focused on small research site challenges, innovation, and collaboration.

Proven strategies and tips for success in the Clinical Research Coordinator certification exam.

A comprehensive resource to prepare for the CRC certification with key topics and practice questions.

Alumni Employment in 81 Countries

Graduates are employed at leading CROs, hospitals, and research institutions worldwide.

Over 1,576 Hiring Organizations

Trusted by top industry employers for clinical research staffing and training.


Similar organizations

Browse all ORGANIZATIONS

JOIN OUR MAILING LIST

Stay Connected with MTEC

Keep up with active and upcoming solicitations, MTEC news and other valuable information.