Teams at Caprion Biosciences

Supports senior project managers in planning and coordinating preclinical and clinical trial projects from initiation through closeout. Tracks schedules, budgets, samples, documentation, risks, deviations, CAPA actions, data quality, and client reporting. Coordinates laboratory workflows, slide QC, testing schedules, system configurations, change orders, secure data transfers, kickoff meetings, and sponsor communications while maintaining audit readiness and compliance with protocols and SOPs.

Supports operational execution of oncology clinical trials by managing site regulatory documents, monitoring visits, action items, site activation, close-out activities, and audit readiness. Coordinates with Project Management, Regulatory Affairs, and Quality Assurance; maintains eTMF and CTMS documentation, manages trial-system access, tracks protocol amendments and informed consent forms, and maintains compliance dashboards.

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.