Jobs at Caprion Biosciences

Supports oncology clinical trial operations by overseeing site regulatory documentation, monitoring visit reports, action item resolution, site activation and close-out activities. Coordinates with Regulatory Affairs, Quality Assurance, and Project Management; manages essential document collection, eTMF readiness, system access, regulatory packages, protocol amendments, and compliance dashboards. Requires strong organization, attention to detail, and full-time onsite attendance.