Senior Clinical SAS programmer

Company:  Katalyst Healthcares & Life Sciences
Location: South Plainfield
Closing Date: 20/10/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
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.

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