Hybrid Director, Program Operations Leader – Internal Medicines

Posted 2 weeks ago

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About the role

  • Director of Program Operations leading strategic management of clinical trial programs at Regeneron. Responsible for overseeing clinical research activities in adherence to regulations and quality standards.

Responsibilities

  • responsible for leadership and overall strategic management of one or more complex programs in Clinical Trial Management (CTM)
  • responsible for clinical operations activities and decisions including quality, timelines and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s)
  • maintain an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or changes that may impact quality, timelines and/or budget; provide clinical program level updates to stakeholders as requested
  • provide operational insight into feasibility, timeline and cost estimates during clinical program/study development
  • oversee clinical study timelines within a clinical program(s)

Requirements

  • A Bachelor’s degree
  • minimum of 12 years relevant in-house sponsor-side industry experience
  • 8 years within clinical operations

Benefits

  • health and wellness programs (including medical, dental, vision, life, and disability insurance)
  • fitness centers
  • 401(k) company match
  • family support benefits
  • equity awards
  • annual bonuses
  • paid time off
  • paid leaves (e.g., military and parental leave) for eligible employees at all levels!

Job title

Director, Program Operations Leader – Internal Medicines

Job type

Experience level

Senior

Salary

$202,000 - $336,600 per year

Degree requirement

Bachelor's Degree

Location requirements

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