Associate

• Arrange and track system access for project team members
• Maintain and quality audit project portals to ensure the most recent document revisions are available
• Assist with preparation and shipment of clinical trial documentation, including Investigator Site File
• Maintain version control and quality control of project documentation
• Submit project documentation to the trial master file
• Track and maintain project-related information, including site medical question and answer logs
• Provide administrative and project tracking support to the clinical project team
• Ensure assigned project tasks are performed timely and accurately

Associate jobs in Serbia

Clinical Trials Associate