Assistant CRA - FSP

Completes study and site management activities as defined in task matrix. Provides in-house support during pre-study assessments and supports site staff with the vendor related qualification process. Verifies document collection and RCR submission status; updates site EDL and verifies site information.

Bachelor's degree in a life science discipline or related field or a Registered Nursing certification. Previous experience in oncology clinical studies is required, preferably in roles such as CTC, PSC, or Study Coordinator. Basic medical knowledge and understanding of medical terminology.