Related skills
r sas cdisc regulatory submissions sdtm📋 Description
- Lead oncology programming for multiple studies.
- Deliver end-to-end programming and study leadership.
- Oversee Tables, Listings, and Figures for reports.
- Coordinate with CROs and vendors for quality.
🎯 Requirements
- 8–12+ years SAS programming in pharma/CRO.
- Expert SAS; strong CDISC SDTM/ADaM knowledge.
- Oncology trials experience and regulatory submissions.
- Strong leadership and cross-functional collaboration.
- Bachelor’s or Master’s in Statistics, CS, Math, or Life Sciences.
- Excellent communication skills.
🎁 Benefits
- Remote work option within the United States.
- Global CRO environment with career growth.
- Collaborate with sponsors and CRO vendors.
- Access to ongoing training and development.
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