Recruiting and screening study participants, obtaining informed consent, collecting and recording clinical data, managing investigational product, coordinating study visits, communicating with IRBs and sponsors, and maintaining regulatory binders.
Clinical Research Coordinators manage the day-to-day operations of clinical trials — ensuring protocol compliance, data integrity, and participant safety. We find the professionals your organisation needs through dedicated retained search — not job boards.
Speak with a retained recruitment specialist today.
🔒 No hard sell · No obligation · Google Meet
Recruiting and screening study participants, obtaining informed consent, collecting and recording clinical data, managing investigational product, coordinating study visits, communicating with IRBs and sponsors, and maintaining regulatory binders.
Bachelor's degree in a health science, CCRP or CCRC certification preferred, and 1–3 years of clinical trials coordination experience. ICH/GCP training and experience with specific therapeutic areas or trial phases are often required.
CRCs who have coordinated Phase II and Phase III trials and maintained FDA audit-ready records are among the most sought-after in clinical research. Sponsor-facing experience differentiates candidates significantly.
Ready to start a search for a Clinical Research Coordinator?
📅 Book a Free Consultation25 min · Google Meet · No obligation
Our retained model delivers a pre-screened, credentialled shortlist within 21–40 days. Start with a free, confidential 25-minute consultation.
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