Hiring a full time (W2/FTE) US based SAS programmer with experience in programming for a contract research organization (CRO) and phases I-IV clinical trials. Offering salary, benefits, 401k etc…
This is remote position.US applicants only. International applicants not accepted.
Duties
- Develop, maintain, and produce SAS code for CRF data, STDM data, and ADaM data.
- Develop, maintain, and produce table/listing/figures
- Ad-hoc Analysis Support.
- CDISC Compliance.
- Integrated Summary of Safety (ISS) programming support – safety summary AdaM data and tables.
- Maintain Summary of Change Documents for efficacy analysis and ad-hoc analysis.
- Review SAP, CRF design, and ISS/ISE plan documents.
- QC datasets, tables, listings, figures
- Reviewer’s Guide experience
- Pinnacle 21 experience
- aCRF experience
- STF (Study Tagging File) experience
Requirement:
- MS in statistics/biostatistics/computer science
- 5 yeas CDISC experience
- SAS system development experience
- NDA experience
- CRO experience preferred.
- Phases I-IV knowledge
- Lives in US