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Key Responsibilities:

  • Lead and oversee end-to-end clinical trial operations from study start-up through close-out.
  • Develop and execute operational plans, timelines, and performance metrics to support successful delivery of assigned studies.
  • Partner closely with Clinical Development, Regulatory Affairs, Data Management, Biostatistics, Safety, and other functions to ensure aligned and efficient trial execution.

Qualifications:

  • Bachelor’s degree in sciences field required; advanced degree preferred.
  • 8+ years of experience in pharmaceutical, biotechnology, or CRO environments in clinical operations.
  • Proven experience managing clinical trials across multiple phases (Phase 1–3), including domestic and international studies.

Centessa Pharmaceuticals

Centessa Pharmaceuticals plc is a new kind of pharmaceutical company with a deconstructed R&D environment that prioritizes data-driven decision-making led by subject matter experts. Their asset-centric model offers a unique R&D logic that has been applied by single-asset companies to improve productivity.

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