IQVIA UK's cFSP is seeking an experienced Clinical Research Associate to perform site monitoring visits across interventional studies in line with GCP/ICH guidelines and contracted scope.
You will work with sites to drive subject recruitment, train site staff on protocol procedures, ensure TMF/isf compliance, and maintain strong communication with the study team. On-site, hybrid work options offered.
Flexible Clinical Research Coordinator – Monitoring & Compliance in Salford employer: Iqvia Uk's Cfsp
IQVIA is an exceptional employer for Clinical Monitoring Associates, offering a dynamic work culture that prioritises career development and flexible working arrangements to support a healthy work-life balance. With a strong commitment to employee well-being and recognition as one of the best places to work in the UK, IQVIA provides unique opportunities for growth and collaboration within a leading global provider of clinical research services.
