Offer summary
Qualifications:
Bachelor’s degree in life sciences or related field, 3-5 years of experience in clinical data management, Experience in IVD or medical device industry preferred, Proficiency in Veeva Vault CDMS is preferred, Strong understanding of regulatory requirements for IVD.
Key responsabilities:
- Oversee clinical trial data management
- Implement comprehensive Data Management Plans
- Ensure data collection and validation processes are accurate
- Generate and review data reports for analysis
- Collaborate with cross-functional teams on IVD trials