IQVIA LLC is seeking a site monitor to perform on-site visits across interventional studies, ensuring adherence to GCP/ICH guidelines. You will drive subject recruitment plans and administer protocol training to sites, maintaining clear communication on project expectations.
The role supports TMF/ISF maintenance and CSF data handling, with ongoing collaboration across the study team. The ideal candidate has 2+ years of independent on-site monitoring experience, knowledge of regulatory
#J-18808-Ljbffr
Clinical Monitoring Specialist — GCP/ICH Focus 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.
