SAS Programmer
We are seeking a highly skilled Statistical Programming Contractor to support clinical development studies within a growing biotech organization. This role partners closely with the Senior Manager and the Director of Statistical Programming and cross‑functional teams to deliver high‑quality analysis datasets and outputs for ongoing trials.
The ideal candidate is a strong hands‑on SAS programmer with experience in CDISC standards and clinical trial data, capable of working both independently and collaboratively.
What You'll Do
- Develop and validate SAS programs for ADaM datasets, tables, listings, and figures (TLFs)
- Support analysis activities per SAPs and study requirements
- Review and QC datasets and TLFs delivered by CRO partners
- Create or review derived dataset specifications and documentation
- Troubleshoot data and programming issues with internal teams and CROs
- Ensure compliance with CDISC (SDTM/ADaM) standards and internal SOPs
- Participate in study team discussions as needed
What We're Looking For
- 3-5+ years of SAS programming experience in pharma, biotech, or CRO environment
- Strong expertise with SAS and clinical trial programming
- Proven experience with CDISC SDTM/ADaM
- Ability to manage multiple tasks in a fast‑paced environment
- Working knowledge of R (nice to have)
- Excellent communication and problem‑solving skills
- W2 workers only
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