IQVIA LLC in the United Kingdom is seeking a site management/monitoring professional to oversee the progress of assigned studies, including regulatory submissions, recruitment, CRF completion and data query resolution. The role requires coordinating with study teams, maintaining TMF/ISF in line with GCP and local requirements, and producing visit reports and follow-up letters.
A Bachelor's degree in a scientific discipline or healthcare is preferred, with on-site monitoring experience.
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Senior Clinical Research Associate – Onsite Monitoring in Broughton 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.
