Clinical Operations Associate Director

New

Skills

Clinical Operations Management CRO Oversight Cross-Functional Team Leadership Global Trial Operationalization ICH-GCP Knowledge Process Excellence Collaboration Project Management Regulatory Compliance Resource Planning Vendor Management

We are seeking an experienced Associate Director for Clinical Operations Standards and Planning to identify operational efficiencies with CROs and vendors, ensuring timely trial delivery. This role involves leading resource planning and developing standards for global clinical trials across various programs.

Key Responsibilities
  • Identify operational efficiencies with CROs and vendors to support trial delivery.
  • Lead Clinical Operations resource planning to ensure timely staffing.
  • Develop and maintain standards for global clinical trials across programs.
  • Collaborate with Process Excellence and QA to standardize study operations.
  • Oversee resource planning to optimize utilization across the organization.
  • Drive end-to-end clinical operations processes with cross-functional teams.
Requirements & Qualifications
  • 12+ years of experience in pharma/biotech Clinical Operations.
  • Bachelor's degree required.
  • Experience overseeing CROs, vendors, and trial consultants.
  • Experience operationalizing large global trials.
  • Strong leadership, communication, and cross-functional influence.
  • Deep knowledge of ICH-GCP, 21 CFR Part 11, and health authority regulations.

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Job Type: Remote

Salary: Not Disclosed

Experience: Entry

Duration: Months

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