Clinical Operations

• Support clinical study teams with administrative and operational tasks
• Manage site payments and clinical trial supplies
• Maintain and organize essential study documentation within electronic systems
• Perform Trial Master File (TMF) related activities to support inspection readiness
• Track, collect, scan, file, and process study documents and Case Report Forms (CRFs)
• Provide limited site-facing support in partnership with Clinical Research Associates
• Work closely with Clinical Research Associates and project teams throughout the clinical trial lifecycle

Explore Clinical Operations Associate at Parexel. Review requirements and application details.