IQVIA LLC is seeking experienced Clinical Research Associates in the UK to monitor study sites and manage site activities in line with the protocol and regulatory requirements.
Responsibilities include site visits, regulatory tracking, and maintaining essential study documentation. Collaboration with the study team and escalation of quality issues are expected. Reading and Manchester locations imply field-based work with potential travel across the UK.
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Clinical Research Associate II – On-Site Monitoring in Manchester 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.
