IQVIA LLC is seeking an on-site Clinical Site Monitor to ensure study sites conduct the protocol per regulatory standards. You will manage monitoring visits, data queries, and site documentation to support project milestones.
Ideal candidates have a bachelor’s in a scientific field or healthcare and at least 2 years of monitoring experience, with strong English communication and IT skills. This full-time role is based in the Reading/ Manchester area and involves regular site travel.
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Senior CRA: Site Monitoring & Study Delivery in Reading 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.
