Senior Manager, Biostatistics

Bristol Myers Squibb

Senior Manager of Biostatistics managing statistical analyses for oncology clinical trials at RayzeBio. Collaborating with multidisciplinary teams to ensure timely and effective execution of study designs and analyses.

Posted 7/3/2026full-timeSan Diego • California, New Jersey • 🇺🇸 United StatesSenior💰 $164,846 - $199,754 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Serve as the study biostatistician for assigned clinical oncology studies, contributing to the development and execution of statistical strategies, study designs, and analyses under the guidance of senior biostatistics leadership.
Collaborate closely with multidisciplinary project teams to ensure timely communication and alignment of objectives.
Help identify and implement solutions to statistical and data analysis issues related to clinical trials and regulatory submissions.
Author and contribute to key statistical documents and outputs, including protocol statistical sections, SAPs, and TLF shells, with review by senior biostatisticians.
Review study-related documents and review/validate vendor deliverables, including CDISC data specifications and TLF/analysis outputs.
Work with internal programmers to support regulatory requests, DSUR/IB updates, and ad-hoc analyses as needed.
Participate in the internal sponsor review of ongoing clinical data.
Support AI initiatives led by the Biometrics AI lead that enhance quality control and operational efficiency.

Requirements

What you’ll need

Ability to work on site in our San Diego Office working Hybrid Work Schedule.
Willing to travel approximately 10% of the time.
Evening and weekend work will be involved.
Strong interpersonal and communication skills, with the ability to collaborate effectively with cross-functional stakeholders.
Able to function in a highly regulated environment and to adhere to all RayzeBio guidelines and SOPs.
Proficiency with statistical programming tools (e.g., SAS and/or R) and working knowledge of CDISC standards (SDTM/ADaM), with the ability to review and interpret key statistical outputs.
Experience working with vendors to help ensure the quality, timeliness, and compliance of biometrics deliverables.
Solid working understanding of GCP, ICH guidelines, and regulatory requirements.
Advanced degree in Statistics or Biostatistics (PhD or MS).
3+ years (PhD) or 6+ years (MS) of biostatistics experience in the pharmaceutical/biotech industry.
Familiarity with AI-enabled tools to improve productivity and work efficiency.
Exposure to innovative/novel clinical trial designs (e.g., adaptive designs).
Working knowledge of Bayesian methods in a clinical development setting.

Benefits

Comp & perks

Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. *Eligibility Disclosure: T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.

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Hard Skills & Tools

BiostatisticsStatistical ProgrammingData AnalysisStatistical Document AuthoringRegulatory SubmissionsBayesian MethodsClinical Trial DesignQuality ControlData ValidationAI-Enabled Tools

Soft Skills

Interpersonal SkillsCommunication SkillsCollaborationProblem SolvingAdaptability