Senior Director, Clinical Operations — Oncology Trials Leader

Revolution Medicines, Inc.

San Francisco (CA)

Sur place

USD 244 000 - 305 000

Plein temps

Il y a 3 jours
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Résumé du poste

Revolution Medicines in Redwood City, CA is seeking a Senior Director of Clinical Operations to lead the design and execution of early-stage clinical studies. You will shape the Clinical Development Plan and oversee trial execution with CROs and sites.

The role requires 12+ years in clinical operations, strong leadership, and extensive experience managing global Phase 1–3 trials under FDA/ICH guidance. Base pay ranges from $244,000 to $305,000 USD and will be set for onsite work.

Qualifications

  • BS/MS in a scientific discipline with 12+ years of clinical operations experience.
  • Minimum 7 years of project and line management experience.
  • Extensive experience leading global phase 1-3 trials within timelines, resources, and budgets.
  • Experience in CRO/vendor selection and external resource management.
  • Strong knowledge of FDA Regulations, ICH Guidelines and GCPs.

Responsabilités

  • Develop and manage the Clinical Development Plan (CDP) including timelines, budgets, and resource needs.
  • Oversee execution of clinical trials, including CRO and site selection.
  • Deploy Clinical Operations staff and establish clear roles for growth.
  • Line management: hiring, performance management and mentorship.
  • Collaborate with Clinical Dev, DMPK, Regulatory, QA, Finance, Legal to achieve study goals.

Connaissances

Leadership
Clinical ops
Vendor management
FDA/ICH/GCP knowledge
Data management

Formation

BS/MS in science

Outils

CRO management
Data management systems

Description du poste

Revolution Medicines in Redwood City, CA is seeking a Senior Director of Clinical Operations to lead the design and execution of early-stage clinical studies. You will shape the Clinical Development Plan and oversee trial execution with CROs and sites.

The role requires 12+ years in clinical operations, strong leadership, and extensive experience managing global Phase 1–3 trials under FDA/ICH guidance. Base pay ranges from $244,000 to $305,000 USD and will be set for onsite work.

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