Perform independent quality control reviews of electronic Trial Master File (eTMF) documentation and provide support for Clinical Trial Management System (CTMS) platforms. Assist project teams with documentation filing, cleanup, and administrative tasks such as meeting agendas and logs.
Lead complex clinical research projects across the full trial lifecycle, including clinical operations, data, and regulatory submission needs. Manage study budgets, timelines, risks, and sponsor expectations to ensure successful project delivery.
