Role OverviewClinical Research Coordinators (CRCs) are key players in the UK’s healthcare and pharmaceutical research ecosystem. They manage the daily operations of clinical trials, ensuring ethical, regulatory, and procedural compliance throughout all phases of a study.
Manage patient recruitment, informed consent, and scheduling
Maintain trial documentation and electronic data capture systems
Coordinate with sponsors, regulatory bodies, and clinical staff
Ensure compliance with MHRA, GCP, GDPR, and NHS protocols
Detail-oriented – Handles complex documentation with precision
Organised – Manages multiple studies, patients, and deadlines simultaneously
Compliance-driven – Understands ethical and regulatory standards in UK trials
Communicative – Coordinates smoothly with internal and external stakeholders
GCP (Good Clinical Practice) certification – mandatory in most UK-based roles
Familiarity with NIHR or HRA regulations
Experience with CRF/eCRF, CTMS, and patient monitoring
Original price was: £37.97.£4.97Current price is: £4.97.
Original price was: £37.97.£4.97Current price is: £4.97.
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Original price was: £37.97.£4.97Current price is: £4.97.
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