Apply on Kit Job: kitjob.ca/job/2g8ufe

Lead programming efforts in oncology clinical trials as a Senior Statistical Programmer. Deliver regulatory-compliant datasets, tables, listings, and figures while collaborating with Biostatisticians and Clinical teams.

In this senior role, you'll manage end-to-end programming and validation processes for clinical trial datasets to ensure they meet regulatory standards. Your extensive experience will be essential in supporting Phases I-III trials, focusing on high-quality output for submissions. You will work closely with various teams to maintain data integrity and client satisfaction.

Key Responsibilities: • Program and validate clinical trial datasets • Develop tables, listings, and figures (TLFs)



• Collaborate with biostatistics and clinical teams • Ensure compliance with regulatory standards • Contribute to high-quality submissions for oncology trials

Requirements: • Master’s degree in Statistics is required • 5+ years in statistical programming for pharma/biotech • Proficient in SAS programming (Base, Macro, SQL) • Familiarity with CDISC SDTM and ADaM guidelines • Experience with regulatory submissions preferred

Elevate your career by contributing to impactful oncology trials and ensuring compliance with high-quality programming standards. #J-18808-Ljbffr

Apply on Kit Job: kitjob.ca/job/2g8ufe

📌 Senior Statistical Programmer for Clinical Trials (Toronto)
🏢 Connect Life Sciences
📍 Toronto