Site Management Associate II

Manage records flow with sites and off-site facilities, prepare regulatory and ethics committee submissions, and coordinate payments. Serve as the main contact for non-trial-participant issues, including vendors and trial supplies, while reviewing site-specific query resolutions and EDC progress. Prepare for and follow up on site audits, organize investigator meetings, and provide on-the-job coaching to junior staff. Arrange trial training for site teams, file trial records in the TMF, and coordinate translation processes for trial records. This role supports a global clinical research company focused on bringing new medicines to patients who need them.