What are the responsibilities and job description for the SDTM/Clinical SAS- Visa Independent position at Shrive Technologies?
- Must have 6-8 yrs of exp in clinical domain
- Strong knowledge of SDTM
- Create advanced SAS macros, templates, and utilities for efficient data processing
- Act as the primary programming point of contact for biostatisticians and study teams
- Perform peer review of code and documentation for accuracy and traceability
- Review CRF (Case Report Form) annotations and data specifications.
- Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines
- Extensive programming experience in a clinical trial environment (CRO/Pharma).
- Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO.
- In-depth knowledge of CDISC standards and regulatory submission requirements