Connect Life Sciences · 11 hours ago
Senior Statistical Programmer
Connect Life Sciences is 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 in compliance with regulatory standards, particularly supporting oncology clinical trials.
Responsibilities
Responsible for the end-to-end programming and validation of clinical trial datasets, tables, listings, and figures (TLFs) in compliance with regulatory standards
Supporting oncology clinical trials (Phases I–III)
Working closely with Biostatisticians, Data Management, and Clinical teams to deliver high-quality outputs for regulatory submissions
Qualification
Required
Master's degree in Statistics required
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
Preferred
Experience with regulatory submissions (FDA, EMA, PMDA) preferred
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
Company
Connect Life Sciences
Connect Life Sciences is a recruitment agency that provides staffing and connects talent and opportunity within Life Sciences.
Funding
Current Stage
Early StageRecent News
2025-09-17
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