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Senior Clinical SAS Programmer
Katalyst Healthcares & Life Sciences
- 🇺🇸 United States
- On-site
- Senior
- 10 months ago
- SAS
- CDISC
10 months ago
Not enough detail in this posting to match
As a Clinical SAS Programmer, you will be responsible for attending multi-disciplinary team meetings to represent the programming function. You will create or review and approve programming plans at study and project levels, providing input on key study-related documents produced by other functions.
Key Responsibilities:
- Developing CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies.
- Creating or reviewing software systems to generate displays of clinical study data as tables, listings, and graphs for electronic submission to regulatory agencies.
- Assisting statisticians by suggesting algorithms to address client analysis requests.
- Developing software validation procedures and test plans
- Minimum years of experience in developing software for clinical trials using the SAS system.
- Skilled in programming with SAS. Knowledge of additional programming languages a plus.
- Good knowledge of statistics and drug development process.
- Experience as a lead programmer for NDAs/BLAs.
- Experience overseeing the work of internal contractors and external vendors (CROs).
Senior Clinical SAS Programmer · Katalyst Healthcares & Life Sciences