Clinical SAS Programmer
WhiteCap Search · Cambridge, MA · 1 mo ago
On-siteScienceContract
Key Responsibilities
- Develop, validate, and maintain SDTM and ADaM datasets in accordance with CDISC standards
- Program tables, listings, and figures (TLFs) for clinical study reports, DSMB packages, and regulatory submissions
- Write and QC SAS macros and programs for data derivations and edit checks
- Collaborate with biostatisticians to implement statistical analysis plans (SAPs)
- Support define.xml and reviewer's guide development for regulatory submissions
- Contribute to programming specifications and standard macro libraries as the client's pipeline scales
Qualifications
- Bachelor's or advanced degree in statistics, computer science, life sciences, or related field
- 3+ years of clinical SAS programming experience in pharma, biotech, or CRO
- Strong command of Base SAS/SAS Macro; SAS/STAT a plus
- Solid working knowledge of CDISC SDTM and ADaM standards
- Experience supporting regulatory submissions (NDA/BLA) a plus
- Comfortable working with lean teams and evolving standards at a growing organization