IQVIA is recruiting a Senior Clinical Research Associate to perform on-site monitoring across clinical trial sites. You will lead site qualification, initiation, monitoring, and close-out visits, ensuring patient safety, data integrity, and regulatory compliance while maintaining strong site relationships.
Applicants should have a life sciences degree and at least 2 years of on-site monitoring experience in CRO/pharma settings, with excellent communication and organizational skills, and the
Senior Clinical Research Associate, CFSP – Global Trials in Salford 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.
