Strategic Manager, Statistical Programming Lead

Regeneron Pharmaceuticals, Inc.

New Jersey

On-site

USD 129,000 - 210,000

Full time

48 hours ago
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Job summary

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

Qualifications

  • 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.

Responsibilities

  • 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.

Skills

Clinical study programming
Leadership
SAS Certification

Education

Master's degree in a relevant field

Job description

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

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