Revolution Medicines is seeking an Associate Director, Clinical Operations to oversee clinical trials, manage CROs and vendors, and lead cross-functional teams. The ideal candidate has 11+ years of direct clinical operations experience, strong leadership and organizational skills, and experience in oncology.
Requirements
- RN or Bachelor's or Master's degree in biological sciences or health-related field required.
- 11+ years direct Clinical Operations experience in the pharmaceutical or biotech industry.
- Minimum of 5 years of project and first-line management experience.
- Experience in oncology.
- Experience in leading and managing global phase 1-3 clinical trials within designated timelines, resources, and budgets.
- Strong working knowledge of FDA Regulations, ICH Guidelines, and GCP.
- Experience with vendor management and CRO oversight.
- Ability to perform complex analysis, draw relevant conclusions, and implement appropriate solutions.
- Ability to pivot, be solution-oriented with consideration to long-term impact on clinical trials, responsibilities, and inspection-readiness.
- Strong analytical, negotiation, and persuasion skills.
- Ability to deal with time demands, incomplete information, or unexpected events.
- Outstanding organizational skills with the ability to multi-task and prioritize.
- Excellent interpersonal, verbal, and written communication skills.
- Decision-making skills.
- Comfortable in a fast-paced company environment and able to adjust workload based upon changing priorities.
- Demonstrate proficiency in Microsoft Office Suite (Outlook, MS Word, Excel, PowerPoint); MS Project and/or Smartsheet a plus.
Benefits
- Generous Paid Time Off
- 401k Matching
- Tuition Reimbursement
- Relocation Assistance