Manager, Statistical Programming

Bristol Myers Squibb • Princeton, NJ

1d • Remote

About The Position

Bristol Myers Squibb is seeking a Manager, Statistical Programming to provide programming expertise to clinical project teams. This role supports the development, regulatory approval, and market acceptance of Bristol Myers Squibb products. The individual will design, develop, and implement technical solutions for analyzing and reporting clinical data using industry tools. Key responsibilities include developing analysis datasets, specifications, and outputs such as safety and efficacy tables, figures, listings, and submission packages. The role also involves supporting electronic data submission activities in compliance with regulatory requirements and collaborating with cross-functional teams and external vendors to ensure quality deliverables, provide programming guidance, and support improvement initiatives within Global Biometrics & Data Sciences (GBDS). This position allows for 100% telecommuting.

Requirements

• Bachelor’s degree or foreign equivalent in Statistics, Biostatistics, Mathematics, Computer Science, Pharmaceutical Science, or a related field, and five (5) years of progressive post-baccalaureate work experience.
• Five (5) years of experience in developing analysis data model (ADaM) specifications and derived datasets.
• Five (5) years of experience in creating SAS programs to generate datasets, tables, listings, and figures.
• Five (5) years of experience using Pinnacle 21 Enterprise to generate regulatory-compliant submission packages.
• Five (5) years of experience applying CDISC standards, MedDRA, NCI CTCAE v5, and WHO Drug Dictionary.
• Five (5) years of experience processing upstream data, including source and SDTM data, for ADaM dataset creation.
• Five (5) years of experience applying knowledge of clinical trial development, statistical programming, and data submissions.
• Five (5) years of experience managing vendors for outsourced programming deliverables.

Responsibilities

• Provide programming expertise to clinical project teams to support the development, regulatory approval, and market acceptance of Bristol Myers Squibb products.
• Design, develop, and implement technical solutions for analyzing and reporting clinical data using related industry tools.
• Develop analysis datasets, specifications, and outputs including safety and efficacy tables, figures, listings, and submission packages.
• Support electronic data submission activities in compliance with regulatory requirements.
• Collaborate with cross-functional teams and external vendors to ensure quality deliverables, provide programming guidance, and support improvement initiatives within Global Biometrics & Data Sciences (GBDS).

Benefits

• Annual discretionary bonus
• Healthcare: 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: Flexible time off (unlimited, with manager approval), 11 paid national holidays (with some exceptions), 160 hours annual paid vacation for new hires (with manager approval), 3 optional holidays, 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Manager