Global Study Associate, Oncology R&D, Early Oncology Clinical

Job description

The Global Study Associate is responsible for supporting the delivery of clinical studies by providing administrative and system support. The Global Study Associate will work across several studies, so a high degree of flexibility is required. The exact accountabilities will differ depending on the exact nature of the clinical program. Responsabilities: Collect, review and track relevant study documents. - Support set-up, maintenance, closeout and archiving of the Trial Master File (TMF). Coordinate regular Quality Checks (QC) and review of the TMF, ensuring continual inspection readiness. - Support production of study documents, ensuring template and version compliance and that relevant documents are ready for publishing in the regulatory document management system. - Set-up, populate and accurately maintain information in tracking systems and communication tools. Support other study team members in the use of these systems. - Manage and contribute to the coordination and tracking of study materials and equipment. - Assist in the tracking and reconciliation of invoices. - Support study team and provide study metrics / reports during the study, audits and regulatory inspections. -...