ICON Strategic Solutions is seeking a Senior Clinical Trial Associate to support site management, regulatory compliance, and GCP adherence across regional trials. You will collaborate with project leaders and vendors in a fast-paced environment to drive study quality.
The role emphasizes coordinating meetings, minute taking, maintaining action logs, tracking site performance, mentoring junior staff, and providing back‑up to the project manager to ensure smooth trial operations.
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Senior Clinical Trial Associate - Site & Study Coordination employer: ICON Strategic Solutions
ICON plc is an exceptional employer located in Reading, offering a dynamic work culture that prioritises quality and compliance in clinical trials. Employees benefit from competitive salaries, comprehensive benefits, and ample opportunities for professional growth through collaboration with cross-functional teams and participation in audits. The company's commitment to excellence and innovation makes it a rewarding place for those looking to make a meaningful impact in the field of clinical research.
