IQVIA LLC is seeking an on-site Clinical Research Associate to monitor trial sites, ensure protocol compliance and maintain regulatory documentation. The role involves coordinating site activation, ongoing monitoring, and data query resolution across assigned studies.
The candidate will work with sites to drive subject recruitment plans, administer protocol training, and maintain effective communication with sponsors and study teams.
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Senior Clinical Research Associate - Onsite Monitoring 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.
