IQVIA LLC is seeking an on-site Clinical Site Monitor to oversee monitoring visits across sites in line with GCP and ICH guidelines. You will establish active communication with sites, implement recruitment plans, and ensure accurate documentation and regulatory compliance.
The role requires expertise in trial conduct, ability to travel, and collaboration with cross-functional teams to ensure smooth study execution and data integrity.
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Senior CRA2: Multi-Sponsor Site Monitoring & Compliance in Broughton employer: IQVIA LLC
At IQVIA, we pride ourselves on being an exceptional employer, particularly for those in the field of Pharmaceutical Development. Our Cambridge location fosters a collaborative and innovative work culture, where you will have the opportunity to influence scientific direction, mentor junior scientists, and engage directly with clients. With a strong focus on employee growth and the integration of cutting-edge AI-enabled approaches, we are committed to supporting your professional development while making a meaningful impact in the pharmaceutical industry.
