Apply on Kit Job: kitjob.ca/job/2g8wg6

We are seeking a highly skilled Senior Statistical Programmer/. This role 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.

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, quick-paced environment.

Apply on Kit Job: kitjob.ca/job/2g8wg6

📌 Senior Statistical Programmer - québec city (Quebec City)
🏢 Connect Life Sciences
📍 Quebec City