What are the responsibilities and job description for the Sr Statistical Programmer 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 (TLFs) in compliance with regulatory standards. The ideal candidate will have extensive experience supporting oncology clinical trials (Phases I–III) and working closely with Biostatisticians, Data Management, and Clinical teams to deliver high-quality outputs for regulatory submissions.
Qualifications
- Education: Master’s degree in Statistics required
Required Skills
- Proficiency in SAS programming (Base, Macro, SQL).
- Strong knowledge of CDISC SDTM and ADaM implementation guidelines.
- 5 years of statistical programming experience in the pharmaceutical/biotech/CRO industry.
- Experience with regulatory submissions (FDA, EMA, PMDA) preferred.
- Lead and Client facing experience preferred
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.