Associate Director, Biostatistics
Bristol Myers Squibb
August 14, 2026
Remote
United States
Clinical Research and Development
Summary:
The Associate Director of Biostatistics will guide the design, execution, and interpretation of statistical analyses for clinical trials to support radiopharmaceutical therapy development.
Job Responsibilities:
- Serve as lead biostatistician for clinical oncology projects; develop and execute statistical strategies, study designs, and analyses.
- Collaborate with multidisciplinary teams to ensure timely communication and alignment.
- Identify and implement solutions to statistical/data analysis issues for clinical trials and regulatory submissions.
- Author/own key statistical documents and outputs (protocol statistical sections, SAPs, TLF shells).
- Review study documents and validate vendor deliverables (CDISC data specifications and TLF/analysis outputs).
- Support regulatory requests, DSUR/IB updates, and ad-hoc analyses; work with internal programmers.
- Participate in internal sponsor review of ongoing clinical data.
- Pilot AI initiatives to enhance quality control and operational efficiency.
- Travel ~10%; evening/weekend work involved.
Skills/Knowledge:
- Strong communication/interpersonal skills to influence cross-functional stakeholders.
- Ability to operate in a highly regulated environment and follow guidelines/SOPs.
- SAS and/or R; working knowledge of CDISC (SDTM/ADaM) and ability to review/interpret outputs.
- Vendor oversight for quality, timeliness, and compliance of biometrics deliverables.
- GCP, ICH, and regulatory requirements understanding.
- Apply AI to improve execution and decision-making.
Basic Requirements:
- PhD or MS in Statistics/Biostatistics.
- 6+ years (PhD) or 8+ years (MS) biostatistics experience in pharma/biotech.
- Experience using AI-enabled tools to improve productivity.
Preferred Requirements:
- Oncology clinical development experience.
- Global regulatory submission experience.
Benefits (as stated):
- Health coverage (medical, pharmacy, dental, vision); wellbeing support programs; 401(k), disability, life insurance, and other financial/protection benefits.
- Paid time off (flexible time off or annual vacation + holidays depending on location/role).
The Associate Director of Biostatistics will guide the design, execution, and interpretation of statistical analyses for clinical trials to support radiopharmaceutical therapy development.
Job Responsibilities:
- Serve as lead biostatistician for clinical oncology projects; develop and execute statistical strategies, study designs, and analyses.
- Collaborate with multidisciplinary teams to ensure timely communication and alignment.
- Identify and implement solutions to statistical/data analysis issues for clinical trials and regulatory submissions.
- Author/own key statistical documents and outputs (protocol statistical sections, SAPs, TLF shells).
- Review study documents and validate vendor deliverables (CDISC data specifications and TLF/analysis outputs).
- Support regulatory requests, DSUR/IB updates, and ad-hoc analyses; work with internal programmers.
- Participate in internal sponsor review of ongoing clinical data.
- Pilot AI initiatives to enhance quality control and operational efficiency.
- Travel ~10%; evening/weekend work involved.
Skills/Knowledge:
- Strong communication/interpersonal skills to influence cross-functional stakeholders.
- Ability to operate in a highly regulated environment and follow guidelines/SOPs.
- SAS and/or R; working knowledge of CDISC (SDTM/ADaM) and ability to review/interpret outputs.
- Vendor oversight for quality, timeliness, and compliance of biometrics deliverables.
- GCP, ICH, and regulatory requirements understanding.
- Apply AI to improve execution and decision-making.
Basic Requirements:
- PhD or MS in Statistics/Biostatistics.
- 6+ years (PhD) or 8+ years (MS) biostatistics experience in pharma/biotech.
- Experience using AI-enabled tools to improve productivity.
Preferred Requirements:
- Oncology clinical development experience.
- Global regulatory submission experience.
Benefits (as stated):
- Health coverage (medical, pharmacy, dental, vision); wellbeing support programs; 401(k), disability, life insurance, and other financial/protection benefits.
- Paid time off (flexible time off or annual vacation + holidays depending on location/role).