Job Title
Senior Manager, Statistical Programming
Overview
At Bristol Myers Squibb you will be the programming expert that clinical project teams rely on, transforming complex, messy clinical data into clear, submission‑ready outputs that regulators trust. You will design and implement technical solutions that directly influence whether a medicine moves forward – or doesn’t. Your expertise in CDISC standards, ADaM specifications, SAS programming, and electronic submissions will have a direct line to patient outcomes. You will be embedded in cross‑functional teams, partnering with statisticians, data managers, clinical scientists, and external vendors within BMS’ Global Biometrics & Data Sciences (GBDS) organization and beyond.Read more: careers.bms.com/working-with-us
Responsibilities
- Analyze, clean, and transform clinical data for regulatory submissions, ensuring compliance with CDISC standards.
- Develop and maintain SAS programs for ADaM datasets and analysis tables.
- Prepare electronic submission components and coordinate e‑submission workflows with appropriate teams.
- Review statistical analysis plans, shape programming strategy, and advise senior stakeholders on risk and resolution.
- Drive process improvements and lead initiatives to increase efficiency across statistical programming practices.
- Collaborate with various functional groups—statisticians, data managers, clinical scientists, and vendors—to streamline work streams.
Bonus points
Experience leading or managing a team of technical professionals.
What’s in it for you
- Real regulatory impact – lead and support electronic submissions for significant regulatory filings.
- Technical depth + strategic influence – review analysis plans, shape strategy, and advise senior stakeholders.
- The chance to build and shape a team – mentor and develop other programmers.
- Work that matters at scale – support trials that change standard care worldwide.
- A platform to drive change – identify inefficiencies, lead improvement initiatives, and influence future practices.
Qualifications
- 7+ years of statistical programming experience in the pharmaceutical or biopharma industry, including hands‑on involvement in major regulatory submissions.
- Deep fluency in SAS, CDISC/SDTM/ADaM standards, and the end‑to‑end clinical data pipeline.
- Understanding of the full drug development lifecycle – from eDC data collection through to TFLs and e‑submission components.
- Strong communication skills; able to hold your own in a room of statisticians, clinicians, and regulatory experts.
- Proactive about spotting problems before they become crises and confident enough to communicate them clearly.
- Hold a degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences.
On-site Protocol
BMS determines where an employee is required to conduct their work based on occupancy type (site‑essential, site‑by‑design, field‑based, remote‑by‑design). Site‑essential roles require 100% of shifts onsite. Site‑by‑design roles may allow a hybrid model with at least 50% onsite.
Supporting People With Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations, and ongoing support. Applicants can request accommodations prior to accepting a job offer. For any inquiries, contact adastaffingsupport@bms.com. Learn more: careers.bms.com/eeo-accessibility.
Candidate Rights
BMS will consider qualified applicants with an arrest or conviction record, pursuant to applicable laws in your area.
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more 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.
Requisition Information
R1602530 : Senior Manager, Statistical Programming
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