Clinical SAS Programmer / Senior Clinical SAS Programmer
Experience: 2-6 Years
Mandatory Skills:
- Clinical SAS Programming
- CDISC Standards (SDTM, ADaM)
- Robust hands-on ADaM Programming
- TLF Development & Validation
- Safety and Efficacy Programming
- SAS Macro Programming
- Define.Xml and Pinnacle 21
- Independent/Scratch Programming
- End-to-End Clinical Trial Experience (Phase II/III)
Preferred Skills:
- Oncology, Neurology, or Immunology studies
- Regulatory Submission Support
- Reviewer/Lead experience
- Strong knowledge of derivations, imputations, and analysis datasets
Key Responsibilities:
- Develop and validate SDTM and ADaM datasets.
- Create and validate TLFs for clinical studies.
- Support efficacy and safety analyses.
- Perform independent SAS programming and validation.
- Ensure compliance with CDISC standards and regulatory requirements.