IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK
Job Summary
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
Matching Summary
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
Skills & Requirements
Must-have
On-site monitoring experience
GCP and ICH guidelines knowledge
Clinical trial protocol management
Subject recruitment planning
Nice-to-have
Career development opportunities
Cutting edge medicines
Data pool access for efficiency
Key Requirements
Minimum 6 months independent on-site monitoring
Life science degree or equivalent industry experience