Hybrid Director, Program Operations Leader – Internal Medicines

Posted 6 hours ago

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About the role

  • Director of Program Operations leading complex Clinical Trial Management programs. Overseeing clinical operations within timelines, quality, and budgets for clinical research studies.

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
  • interacts with senior level management, external vendors, collaboration partners and clinical study personnel
  • 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 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)

Job title

Director, Program Operations Leader – Internal Medicines

Job type

Experience level

Senior

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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