— Course series

Clinical Research Coordinator (CRC) Professional Certification

CRC — Clinical Research CoordinatorRun clinical trial sites with confidence and precision. Designed for site coordinators, study nurses, and investigators, this course teaches protocol execution, informed consent, regulatory documentation, patient recruitment, and site management. Walk away ready to coordinate trials at any global site.
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10 modules

Comprehensive, self-paced curriculum covering every core competency.

CPD-certified

Accredited programs recognized by sponsors, CROs, and health authorities.

10 Expert instructors

Direct access to working CRAs and CRCs who guide your real-world growth.

12 months access

Full year of platform access from enrollment — learn on your schedule.
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— What's included

Run clinical trial sites with confidence

CPD-certified training for Clinical Research Coordinators — from informed consent and source documentation to monitoring visits, safety reporting, and study close-out. Built for the realities of running a busy research site.

  • Site operations from SIV to close-out

    Ten modules covering recruitment, screening, source documentation, IP and pharmacy management, and the daily craft of running a compliant site.

  • Ethics, consent & GCPAssessments - Exams

    Master ICH-GCP E6 (R2) for the site — informed consent for vulnerable populations, delegation logs, PI oversight, and the safeguards that protect every participant.

  • Site-Ready Coordinator Skills

    Build the informed consent, source documentation, IP accountability, and visit-coordination skills sites and sponsors hire for — mapped to ICH‑GCP E6(R3), FDA, and IRB expectations.

Course Curriculum

Bundle offer