Offer summary
Qualifications:
University or college degree in life sciences, Clinical Data Management experience, Fluent in English (oral and written), Attention to detail for quality assurance, Ability to manage time flexibly on projects.Key responsabilities:
- Provide study level CDM administrative support
- Manage study start-up, conduct, and closeout phases
- Conduct study status reporting and collaboration with vendors
- Ensure compliance with Quality standards and Trial Master File
- Perform User Acceptance Testing of electronic Data Capture systems
