IQVIA LLC seeks a skilled clinical monitoring professional to conduct on-site visits across sites, ensuring protocol adherence and regulatory compliance. You will manage site communications, training, and quality issues, contributing to project success.
The role requires travel, strong knowledge of GCP/ICH, and experience coordinating regulatory submissions and data handling across multiple studies. Join IQVIA to support innovative medical treatments and patient outcomes.
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Senior CRA: Multi-Sponsor Site Monitoring & Compliance 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.
