Offer summary
Qualifications:
Bachelor's degree in a technical field with 2-5 years of experience or Master's degree with 0-2 years of experience, Proficient in SAS programming and macros, Extensive experience with data automation systems, Competent in designing clinical databases within EDC systems, Mandatory: SAS base certification.
Key responsabilities:
- Develop and validate clinical trial databases and CRFs
- Execute SAS edit checks, conduct data validation, and oversee statistical analyses
- Organize documentation and communicate data management requirements
- Provide training and support for EDC systems to clinical site personnel
- Create and supervise project-specific data management plans