Job title: Clinical SAS Programmer
Company: Katalyst Healthcares & Life Sciences
Job description: Responsibilities:
- Perform data manipulation, analysis and reporting of clinical trial data.
- Program and generate tables, listings, and graphs (TLGs).
- Participate in the review of statistical analysis plans, table specification, develop specification for SDTM and ADaM data sets.
- Review, and comment on CRFs, annotated CRFs, and edit checks and related documents.
- Participate in study team meetings and address issues that may affect statistical programming.
- Validate and document SAS programs and output.
- Create SDTM and ADaM Datasets and related documentation.
Requirements:
- 5+ years of statistical programming experience in the pharmaceutical/biotech industries, strong tenure with Sponsor companies.
- Strong submissions experience (BLA, NDA/sNDA and EMA) and end to end programming experience.
- Knowledge and experience working with CDISC Standards (MUST have expertise in both SDTM/ADaM, developing specifications for both).
- Demonstrated ability performing all levels of programming activities for a clinical project.
- Experience working in the Cardiovascular or Neuromuscular areas is a plus.
Expected salary:
Location: Downey, CA
Job date: Thu, 19 Sep 2024 01:17:52 GMT
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