Sr. Clinical Research Associate (Temporary)

This contract position is responsible for ensuring that data collected for clinical studies is accurate, plausible, and traceable to source documentation, assisting in site management, and clinical study materials development. Primary responsibilities include supporting site identification, qualification, initiation, routine monitoring, and close-out activities. The role also involves conducting site monitoring visits, performing Source Data Verification (SDV), and ensuring timely completion of case report forms (CRFs). Additional responsibilities encompass tracking regulatory document submissions, IRB approvals, recruitment progress, and data collection timelines. Ensuring the maintenance of essential regulatory documents, providing GCP training to site staff, overseeing investigational product tracking, and participating in internal team meetings are also key aspects of the role.