Description
The Senior CRA I leads clinical study site monitoring and site management, including routine and closeout monitoring, initiation and pre-study visits, source-document review, data monitoring, audit readiness, registry administration, vendor coordination, SAE follow-up, and project coordination. The role may serve as a Local Project Coordinator or Lead CRA, supervise junior staff, and travel 60–80% overnight. Candidates need a life-science or allied-health degree or equivalent clinical research experience, three years of clinical monitoring experience, advanced monitoring and site-management skills, strong communication and computer skills, and a valid driver's license.
