Not specified (assumed to be hybrid or onsite based on role nature).
Independent on-site monitoring experience
Good clinical practice gcp knowledge
Ich guidelines expertise
IQVIA is seeking experienced Clinical Research Associates for a sponsor-dedicated role in the UK, focusing on site monitoring and regulatory compliance. The position offers opportunities for career development and involves working with cutting-edge medical treatments
Job Summary
IQVIA is recognized as #1 in its category on the 2025 Fortune World's Most Admired Companies list for the fourth consecutive year.
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out visits in accordance with regulatory requirements.
Candidates will work with sites to adapt, drive, and track subject recruitment plans to enhance predictability and project performance.
Matching Summary
Match Score: 85
IQVIA is seeking experienced Clinical Research Associates for a sponsor-dedicated role in the UK, focusing on site monitoring and regulatory compliance. The position offers opportunities for career development and involves working with cutting-edge medical treatments.
Skills & Requirements
Must-have
Independent on-site monitoring experience
Good Clinical Practice GCP knowledge
ICH guidelines expertise
Site recruitment plan management
Trial Master File maintenance
Nice-to-have
Flexible to travel to sites
Cutting edge medicines development
Significant data pools access
Career development opportunities
Collaborative team environment
Key Requirements
Minimum 6 months independent on-site monitoring
Life science degree or equivalent industry experience
UK work authorization required (no visa sponsorship)