What are the responsibilities and job description for the Senior Statistical Programmer, Oncology position at Connect Life Sciences?
We are seeking a highly skilled Senior Statistical Programmer. This is a lead role and will be responsible for the end-to-end programming and validation of clinical trial datasets, tables, listings, and figures in compliance with regulatory standards. The ideal candidate will have extensive experience supporting oncology clinical trials (Phases I–III).
Required Skills
- 8-10 years of statistical programming experience in the pharmaceutical/biotech/CRO industry.
- Experience with regulatory submissions
- Efficacy Programming
- Lead and client facing experience preferred
- Strong knowledge of CDISC SDTM and ADaM
Preferred Skills
- Excellent problem-solving skills, attention to detail, and ability to manage multiple priorities.
- Strong communication skills and ability to work in a collaborative, fast-paced environment.