global study associate onco (temp big pharma).

• Collect, review and track relevant study documents.• 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.• Lead the practical arrangements and contribute to the preparation of internal and external meetings e.g. study team meetings, monitor meetings, investigator meetings and advisory boards.• Liaise with internal and external participants and/or vendors. Track approvals and completion of required documents.• Prepare and distribute study-related correspondence. Contribute to and distribute material for meetings, newsletters and websites. ...