Related skills
r sas regulatory submissions oncology cdisc sdtm📋 Description
- Lead programming activities for oncology trials across studies.
- Develop, validate, and maintain SDTM/ADaM datasets per CDISC.
- Oversee Tables, Listings, and Figures (TLFs) for study reports.
- Act as programming lead for assigned studies; manage timelines.
- Provide SAS programming expertise for complex data derivations.
- Review traceability, consistency, and quality of deliverables.
🎯 Requirements
- 6 to 10+ years SAS programming in pharma/biotech or CRO.
- Expert-level proficiency in SAS.
- Strong CDISC SDTM and ADaM standards knowledge.
- Oncology trial experience and regulatory submissions.
- Experience with define.xml, annotated CRFs, reviewer guides.
- Excellent communication and cross-functional collaboration.
Meet JobCopilot: Your Personal AI Job Hunter
Automatically Apply to Data Jobs. Just set your
preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.
Help us maintain the quality of jobs posted on Empllo!
Is this position not a remote job?
Let us know!