Clinical Research Associate II Yorkshire
Core
On-site Clinical Research Associate monitoring Phase I–Ib clinical trials in a dedicated Clinical Research Unit, focusing on real-time data review and study quality.
Role type
Clinical Research Associate II (IC)
Builds
Clinical trial data integrity and protocol compliance for early-phase drug development
Domain
Life Sciences / Clinical Pharmacology
Required skills
Independent site management monitoring, Pre-study/Site Initiation/Process/Routine/Close-out visits, Source data review, Protocol compliance, SAE reporting, ICH GCP guidelines
Preferred skills
None stated
Technologies
eSource, EDC
Responsibilities
Monitor Phase I–Ib studies across CRU and UK sites, Perform all monitoring visit types, Review source data and protocol compliance, Collaborate with clinical and lab teams
Seniority
Mid-level, hands-on IC
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