Clinical Trials Associate
Core
Provide administrative and project coordination support to clinical project teams to ensure trial activities and documentation are managed accurately and on time.
Role type
Administrative Clinical Trials Associate
Builds
Clinical trial operations and documentation
Domain
Clinical Research / Healthcare
Required skills
Document management, Version control, Project tracking, ISF maintenance, TMF management, System access coordination, Quality checks, Microsoft Office proficiency
Responsibilities
Coordinate and track system access for clinical project team members, Maintain project portals and perform quality checks, Support preparation and shipment of clinical trial documentation, Assist with preparation and maintenance of Investigator Site Files (ISFs), Submit and maintain documentation within the Trial Master File (TMF), Track and update project-related information including site medical logs, Provide day-to-day administrative and project tracking support, Monitor assigned tasks to ensure timely completion
