Offer summary
Qualifications:
Bachelor's degree in a technical field, Master's degree in a related discipline, In-depth expertise in SAS programming, Experience creating CRFs and data management documentation, Familiarity with data visualization tools like Power BI.
Key responsabilities:
- Design and validate clinical trial databases
- Program SAS edit checks and macros
- Maintain and organize CRFs and other documentation
- Deliver training on EDC systems
- Develop and supervise project-specific data management plans