Job Summary
A research institute is seeking a Telecommute Statistical Programming Manager.
Must be able to:
- Assist with the oversight of SAS programming personnel
- Train SAS programmers regarding applicable regulatory guidelines
- Assist with resource allocation and with the development of business proposals
Must meet the following requirements for consideration:
- Master’s in technology, statistics, pharmaceutics or related field
- 5 years of SAS programming experience with clinical trial data
- 3 years of supervisory OR 5 years of project lead experience in a CRO
- Excellent working knowledge of CDISC SDTM and ADaM Implementation Guidelines
- Thorough knowledge of International Conference on Harmonisation Good Clinical Practice
- Excellent knowledge of regulatory requirements and drug development process
