IQVIA Biotech is seeking an experienced On-site Clinical Monitor to oversee oncology studies, conduct site visits, and ensure protocol and regulatory compliance. You will train site staff, manage recruitment plans, and liaise with the study team to drive project success.
Applicants should have 3–4 years of on-site monitoring experience, strong GCP/ICH knowledge, and proficiency in MS Office; fluent English is required. This role is based in the UK and involves extensive site interactions.
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Senior CRA, Oncology Monitoring & Site Management 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.
