Senior Clinical SAS programmer - Katalyst Healthcares & Life Sciences
South Plainfield, NJ 07080
About the Job
Responsibilities and Requirements:
- Program and validate SDTM and ADaM datasets following approved dataset specifications for CSRs, ISS, and Client.
- Archive clinical trial data (SDTM and ADaM datasets).
- Perform CDISC standard compliant checks on SDTM and ADaM datasets.
- Resolving day-to-day work-related issues and productivity of statistical programming work.
- Perform overall quality/consistency review of statistical TLGs.
- Master's or Ph.D. degree in Statistics, Biostatistics, Epidemiology, and Computer Sciences.
- 6 years + experience in Clinical Trial Programming or 8 years+ if Bachelor' Degree.
- Previous experience working within a Full-Service CRO (Phase I-IV).
- Experience with Programming and validating SDTM and ADaM datasets.
Source : Katalyst Healthcares & Life Sciences
