Medidata RAVE - Biotech / Pharma

- Must have a Bachelor's degree and 2-3 years of experience in database management and SAS programming applied to clinical trials data.
- Significant expertise and at least 2 years of experience in building databases in Medidata Rave is a must with a biotech/pharma/CRO

Must be proficient in writing edit checks

Duties / Responsibilities:

- Design computerized databases in Medidata RAVE in accordance with standardized database structures and/or study specific annotated CRF.
- Design data entry screens.
- Write, execute and test PL SQL and/or SAS edit check programs to check the data for syntax errors, logical inconsistencies, and protocol violations.
- Generate data listings to facilitate data review performed by the clinical data managers.
- Convert databases from the data entry platform into the SAS format and prepare the SAS databases for analysis.
- Design quality control measures and conduct database audits to ensure the integrity of the clinical trial databases.
- Perform other duties as required.

To find out more about Real Staffing please visit www.realstaffing.com