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Biostatistical Programmer Jobs (NOW HIRING)

The Biostatistical Data Programmer will work under the guidance of a Biostatistician/Data Scientist in database management and data sciences to support the development, programming and maintenance of ...

Role OverviewThe Sr. Manager, Biostatistician/Programmer plays a critical hands-on role in supporting Legend Biotech's clinical development programs by transforming clinical trial data into high ...

Biostatistical Programming Manager What you will do Let's do this. Let's change the world. In this ... as a lead programmer for studies and projects, such as Data Access Plan (DAP) activities ...

Biostatistical Programming Manager What you will do Let's do this. Let's change the world. In this ... as a lead programmer for studies and projects, such as Data Access Plan (DAP) activities ...

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Biostatistical Programmer information

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$84.5K

$147.3K

$249K

How much do biostatistical programmer jobs pay per year?

As of Sep 9, 2026, the average yearly pay for biostatistical programmer in the United States is $147,292.00, according to ZipRecruiter salary data. Most workers in this role earn between $125,000.00 and $160,000.00 per year, depending on experience, location, and employer.

What is a biostatistical programmer?

Biostatistical Programmers are professionals who use statistical programming languages, such as SAS, R, or Python, to analyze biological and clinical data. They support clinical trials and public health research by managing datasets, performing statistical analyses, and generating tables, listings, and figures for reports or regulatory submissions. Their work is essential in ensuring data quality and integrity, as well as interpreting results to support scientific conclusions. Biostatistical Programmers often collaborate with statisticians, data managers, and clinical teams in pharmaceutical, biotechnology, or research organizations.

How does a biostatistical programmer typically collaborate with clinical research teams during a study?

Biostatistical Programmers work closely with clinical researchers, data managers, and statisticians throughout the lifecycle of a clinical study. They are responsible for transforming raw clinical trial data into analyzable datasets, generating tables, listings, and figures, and ensuring data integrity. Collaboration often involves participating in regular team meetings to discuss data requirements, timelines, and any challenges that arise during statistical programming. Effective communication and teamwork are essential, as programmers must often clarify statistical analysis plans and adapt to evolving project needs.

What are the key skills and qualifications needed to thrive as a biostatistical programmer, and why are they important?

To thrive as a Biostatistical Programmer, you need a solid background in statistics, programming (typically in SAS, R, or Python), and a relevant degree in biostatistics, mathematics, or a related field. Proficiency with clinical trial data management systems, statistical analysis software, and familiarity with regulatory standards such as CDISC are essential. Attention to detail, problem-solving skills, and effective communication help distinguish top performers in this role. These skills ensure accurate data analysis, regulatory compliance, and clear reporting of clinical trial results, which are critical for advancing medical research.

What cities are hiring for Biostatistical Programmer jobs?

Cities with the most Biostatistical Programmer job openings:

Who are the top companies hiring for Biostatistical Programmer jobs?

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What states have the most Biostatistical Programmer jobs?

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What are popular job titles related to Biostatistical Programmer jobs?

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Infographic showing various Biostatistical Programmer job openings in the United States as of August 2026, with employment types broken down into 83% Full Time, 6% Part Time, 10% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $147,292 per year, or $70.8 per hour.

Director, Biostatistical Programming

San Diego, CA • On-site

Bristol-Myers Squibb
Scientific Research and Development Services • 10K+ employees

$227K - $275K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 9 days ago


Bristol Myers Squibb rating

8.2

Company rating: 8.2 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

33rd of 86 rated pharmaceutical


Job description

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer.

Here, you'll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact-on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: https://careers.bms.com/rayzebio/ The Director of Biostatistical Programming at RayzeBio will be accountable for development of clinical study related deliverables and timelines, oversee study vendors' programming deliverables, and support company internal requests

The successful candidate will report to the Head of Biostatistical Programming. Job Responsibilities Essential duties and responsibilities include the following. Other duties may be assigned.

Oversee vendors' activities, and review vendors' deliverables to ensure quality Participate in reviewing, analyzing, and reporting clinical trial data and generating outputs to support DSUR/IBs, publications, FDA meeting briefing documents, and other internal ad-hoc requests. Collaborate with cross-functional teams to review critical study documents and perform data reviews for ongoing studies Oversee CDISC data package development for clinical studies to support CSRs and future regulatory submissions Support head of Biostatistical Programming in Establish programming and QC processes, and create related SOPs Support head of Biostatistical Programming in Develop and maintain SAS programming infrastructure and process to ensure the quality and compliance in statistical programming deliverables Create SAS macros/applications to streamline processes and enhance efficiency Leverages AI to drive program, portfolio, or functional performance through prioritization and scaled adoption Education and Experience A bachelor's degree required in statistics, mathematics or equivalent with at least 15 years' experience in pharmaceutical industry; or a master's degree in statistics or computer science with at least 12 years' programming experience is preferred. Oncology therapeutic area experience required.

Proven ability to manage CRO relationships and oversee programmed deliverables. Advanced skills in SAS programming and statistical reporting. In-depth knowledge of CDISC standards for SDTM, ADaM and FDA electronic data submission requirements.

Advanced knowledge with FDA and ICH regulations and guidelines, and clinical trial methodologies. Good written and verbal communication skills. Be able to work productively in a fast-paced collaborative environment.

Willing to travel approximately 10% of the time. Evening and weekend work will be involved. Physical demands While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear.

The employee must occasionally lift and/or move up to 20 pounds. Specific vision abilities required by this job include close vision and distance vision. Work Environment The noise level in the work environment is usually moderate.

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Compensation Overview: San Diego - RayzeBio - CA: $227,418 - $275,577 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis.

Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment

Our benefits include: 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: The 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. RayzeBio and Bristol Myers Squibb RayzeBio was acquired by Bristol Myers Squibb (BMS) in 2024 and is a wholly-owned subsidiary of BMS; however, RayzeBio will continue to operate as a standalone organization. Supporting People with Disabilities BMS and RayzeBio are dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles.

Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement

Candidate Rights BMS and RayzeBio will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response

R1603683 : Director, Biostatistical Programming


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About Bristol-Myers Squibb

Sourced by ZipRecruiter

Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.

Industry

Scientific research and development services and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US