Offer summary
Qualifications:
Bachelor’s degree in a scientific discipline, 1-2 years of experience in clinical operations, Proficient in Microsoft Office applications.Key responsabilities:
- Support clinical operations tasks and compliance checks
- Assist with clinical trial documentation and tracking tools
- Maintain and contribute to the Trial Master File (TMF)
- Coordinate site materials, training, and internal/external meetings
- Build relationships with functional teams and stakeholders