IQVIA is seeking a Clinical Research Associate to oversee monitoring of assigned studies, ensuring regulatory compliance and timely data capture. The role involves coordinating site activities, managing TMF/ISF documents, and liaising with the study team to support study execution.
Applicants should have a life sciences degree, at least 2 years of on-site monitoring experience, and strong knowledge of GCP/ICH guidelines, with proficient English communication and Microsoft Office skills.
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Senior Clinical Site Manager, 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.
