Senior Manager, Statistical Programming — Onsite Leadership

BioSpace; New Jersey; Presencial; USD 151 000 - 246 000; Tempo integral

Resumo da oferta

Regeneron is seeking a Senior Manager, Statistical Programming to provide technical leadership across project teams, driving high-quality programming deliverables from single studies through regulatory approval and product launch.

Location options include Warren, NJ or Cambridge, MA with onsite work model. The role emphasizes mentorship, collaboration with global teams, and sponsorship of key regulatory submissions.

Qualificações

• Advanced SAS programming in a clinical data environment.
• Strong understanding of clinical trial principles and regulatory submission requirements.
• Proven ability to lead global, cross-functional teams.
• Experience managing multiple concurrent projects and mentoring junior programmers.
• Preferred knowledge of additional programming languages such as R or Python.

Responsabilidades

• Lead programming support across multiple studies, ensuring timely, high-quality deliverables.
• Coordinate programming documentation and specifications, following established standards.
• Champion company values through excellence, collaboration, and accountability.
• Communicate proactively with study and project teams to clarify requirements and guide programmers.
• Lead submission-ready programming deliverables for global regulatory filings.
• Drive department goals and mentor/direct reports through goal-setting and coaching.

Conhecimentos

Advanced SAS programming

Cross-functional leadership

Mentoring

Project management

Communication

Formação académica

MS or BS in Statistics/CS/Math/Engineering/Life Science

Ferramentas

SAS

R or Python (preferred)

Descrição da oferta de emprego

Regeneron is seeking a Senior Manager, Statistical Programming to provide technical leadership across project teams, driving high-quality programming deliverables from single studies through regulatory approval and product launch.

Location options include Warren, NJ or Cambridge, MA with onsite work model. The role emphasizes mentorship, collaboration with global teams, and sponsorship of key regulatory submissions.