Sr/CRA I/II - UK (numerous locations)
Core
Conducting clinical monitoring and site management for pharmaceutical trials to ensure protocol compliance, data accuracy, and subject safety.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial programs for commercial and government clients
Domain
Life Sciences / Clinical Research
Deliverable
client delivery
Required skills
Risk-based monitoring, protocol compliance, regulatory knowledge (ICH-GCP), data review (SDR/SDV/CRF), root cause analysis, site relationship management, audit readiness
Preferred skills
None stated
Technologies
Clinical Trial Management Systems (CTMS)
Responsibilities
Monitor investigator sites using risk-based approaches, assess investigational product inventory, document observations and deficiencies, track trial status and progress, ensure study system updates, participate in investigator payment processes
Seniority
Senior, hands-on IC
