IQVIA is hiring an experienced Clinical Research Associate in the UK to conduct on-site monitoring visits and support study execution. You will ensure adherence to GCP/ICH, manage site communications, and track regulatory submissions and data queries.
The role requires a life science degree or equivalent experience, travel flexibility, and the ability to collaborate across study teams to drive site performance and patient safety. IQVIA offers world-class training and career development.
#J-18808-Ljbffr
Full job description from WhatJobs. Apply for this role →
Langley
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory…
Reading
Join Us on Our Mission to Drive Healthcare ForwardIQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.With…
Manchester
Escalate quality issues as appropriateManage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and…
Slough, Berkshire
IQVIA UK's Site Management (multi-sponsor) team is growing and seeking junior and experienced Clinical Research Associates.
Manchester, Lancashire
IQVIA UK's Site Management (multi-sponsor) team is growing and seeking junior and experienced Clinical Research Associates.
Lancashire
IQVIA UK's Site Management (multi-sponsor) team is growing and seeking junior and experienced Clinical Research Associates.
Worked with Verifera as a candidate or employer? Your honest review helps the next person trust verified hiring.