Manager, Statistical Programming - Internal Medicine

Regeneron Pharmaceuticals, Inc.; New Jersey; Presencial; USD 129.000 - 210.000; Jornada completa

Descripción de la vacante

Regeneron Pharmaceuticals, Inc. invites applications for a Manager, Statistical Programming to join our Statistical Programming team.

You will lead programming deliverables from a single study through regulatory approval, product launch, and annual reports, collaborating with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis and reporting. This role requires a Master's degree with extensive experience in clinical study programming, strong organizational

Formación

• 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.

Responsabilidades

• Lead programming deliverables from a single study through regulatory approval and launch.
• Develop and QC tables, listings, and graphs in support of analysis requirements.
• Manage programming effort and track progress of deliverables, including complex ad hoc requests.
• Serve as programming representative on a multidisciplinary study team.
• Plan resources for the therapeutic area or department and contribute to hiring.

Conocimientos

Clinical study programming

Leadership

SAS Certification

Educación

Master's degree in a relevant field

Descripción del empleo

Build Our Future Together

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. 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.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & Where

• Location: Warren, NJ or Cambridge, MA
• Work model/flexibility: Onsite

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

#statprogregn

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

$128,600.00 - $210,000.00