Manager, Statistical Programming - Internal Medicine
Regeneron Pharmaceuticals
Summary
We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables from a single study through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis and reporting.
Job description
Discover your role
- Develop expertise within a therapeutic area or standard tool, working independently to coordinate and oversee project deliverables
- Lead the development and quality control of tables, listings, and graphs in support of analysis requirements
- Manage programming effort, tracking progress and completion of deliverables, including complex ad hoc requests
- Serve as programming representative on a multidisciplinary study team, ensuring timely support through regulatory approval and launch
- Partner with management to determine resource requirements for your therapeutic area or department
- Contribute to hiring by reviewing resumes and screening candidates for contractor and permanent roles
- Provide feedback to management on team members' contributions to support performance evaluations and goal-setting
- Advise direct reports on procedures for data, records, and information retention
- Enjoy working with minimal supervision and taking ownership of complex deliverables
- Communicate clearly with cross-functional, multidisciplinary teams
- Think analytically and stay organized when managing multiple priorities and timelines
- Take initiative in developing deep expertise within a specialized area
- Bring a collaborative mindset to hiring, feedback, and team development
- Adapt easily to shifting priorities, including last-minute requests from senior leadership
- Approach quality and documentation with rigor in a regulated environment
This role requires
- Master's degree with 6+ years (or BS 7+) of relevant work experience
- Proven experience leading programming deliverables within a clinical study team
- Experience providing input on hiring, feedback, and performance evaluation
- Strong organizational and documentation skills within a regulated environment
Nice to have
SAS Certification
Requirements
- Master's degree with 6+ years (or BS 7+) of relevant work experience
- Proven experience leading programming deliverables within a clinical study team
- Experience providing input on hiring, feedback, and performance evaluation
- Strong organizational and documentation skills within a regulated environment
- SAS Certification (nice to have)
Benefits
- Annual bonuses
- Incentive plans
- Equity awards
- Pension or retirement benefits
- 401(k) company match
- Health and wellness programs
- Fitness centers
- Insurance benefits
- Paid time off
- Family support benefits
Company overview
Regeneron Pharmaceuticals is a leading American biotechnology company founded in 1988 and headquartered in Tarrytown, New York. The company specializes in inventing, developing, and commercializing life-transforming medicines for people with serious diseases. Regeneron is renowned for its innovative antibody technologies and has developed several groundbreaking therapies, including EYLEA® for retinal diseases, DUPIXENT® for inflammatory conditions, and the COVID-19 antibody cocktail REGEN-COV®. The company operates with a strong focus on research and development across multiple therapeutic areas including ophthalmology, oncology, cardiovascular diseases, and rare genetic disorders. Regeneron's proprietary VelocImmune® technology platform enables the rapid generation of fully human monoclonal antibodies. With over 15,000 employees globally and annual revenues exceeding $14 billion, Regeneron has established itself as a major force in the biotechnology industry, consistently ranking among the top-performing pharmaceutical companies and maintaining a robust pipeline of investigational therapies.