Associate Director, Clinical Operations Compliance & Training

Revolution Medicines

Redwood City, California, United States
Base: $186,000 - $233,000 usd; bonus/equity: compe...
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10+ years clinical compliance experience
Strong knowledge of fda regulations and ich guidelines
Experience developing clinical sops and wis
** Revolution Medicines is seeking an Associate Director, Clinical Operations Compliance & Training in Redwood City, California. This role focuses on leading compliance initiatives, developing clinical policies, and enhancing training programs in a late-stage clinical oncology environment. **

Job Summary

  • Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers.
  • The role requires leading the development of GCP systems, ensuring inspection readiness, and serving as a subject matter expert for clinical operations compliance.
  • Candidates will manage a team responsible for hiring, performance management, and delivering training programs on RevMed standards and regulatory requirements.

Matching Summary

Match Score: 75

** Revolution Medicines is seeking an Associate Director, Clinical Operations Compliance & Training in Redwood City, California. This role focuses on leading compliance initiatives, developing clinical policies, and enhancing training programs in a late-stage clinical oncology environment. **

Salary

Base: $186,000 - $233,000 USD; Bonus/Equity: Competitive cash compensation and robust equity awards; Benefits: Strong benefits and significant learning and development opportunities

Skills & Requirements

Must-have

  • 10+ years Clinical Compliance experience
  • Strong knowledge of FDA Regulations and ICH Guidelines
  • Experience developing Clinical SOPs and WIs
  • Expertise in Good Clinical Practices (GCP)
  • Ability to lead Mock and Regulatory Authority inspections

Nice-to-have

  • Oncology experience in early or late stage trials
  • Line management and mentorship capabilities
  • Familiarity with Ex-US regulations like EMA and MHRA
  • Proficiency in MS Project and Smartsheet
  • RN or Master's degree in biological sciences

Key Requirements

  • Bachelor's degree in biological sciences or health-related field
  • 10+ years direct Clinical Compliance or Quality Assurance experience
  • Demonstrated experience authoring Clinical and cross-functional SOPs

Work Rights

Not specified

Tailored Resume

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