At IQVIA Biotech, we partner with visionary biotech companies to transform innovation into patent impact. With dedicated teams, deep therapeutic expertise, and a biotech tailored model, we accelerate clinical development from early phase through global registrational studies. The successful candidate must be based in a commutable distance to Paris.

**Responsibilities**

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of st...