Senior Clinical Research Associate I (SCRA I)

Independently manage and monitor assigned investigator sites from initiation to database lock. Partner with Site Care Partners on feasibility and site selection processes, and conduct Site Initiation Visits. Mentor and train Clinical Research Associates as assigned, and identify and resolve complex investigator site issues.

Bachelor’s degree in Life Sciences or a professional degree in nursing, pharmacy, or medical background. Minimum of 3 years of relevant experience in clinical research site monitoring, with a preference for 2 years in Oncology. Fluency in English and the native language of the country you will work in.