Clinical Trials Manager

Revolution Medicines, Inc.

California (MO)

On-site

USD 120,000 - 180,000

Full time

12 days ago
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Job summary

Revolution Medicines in Redwood City, CA is seeking a Clinical Trial Manager to oversee Phase I-III oncology clinical operations and CRO oversight, driving study execution across programs.

Responsibilities include vendor management, site visits, IP reconciliation, and leading clinical trial teams while ensuring GCP/ICH/FDA compliance and high-quality documentation. The role requires collaboration with cross-functional teams and travel up to 25%.

Qualifications

  • BS/MS in life sciences or equivalent.
  • 5+ years in clinical operations, preferably in oncology.
  • Strong knowledge of FDA, ICH, and GCP guidelines.
  • Vendor management experience in CRO/vendor oversight.

Responsibilities

  • Manage clinical vendors and CROs ensuring alignment with study goals.
  • Ensure trial compliance with GCP/ICH/FDA regulations and quality standards.
  • Develop and review study documentation including protocols and ICFs.
  • Conduct site visits, oversee investigational product reconciliation, and drug accountability.
  • Lead clinical trial teams and cross-functional study governance.

Skills

Clinical trial management
Vendor management
CRO oversight
GCP/ICH/FDA knowledge

Education

BS/MS in life sciences

Job description

Role

Clinical Trial Manager overseeing Phase I-III oncology clinical operations at Revolution Medicines, focusing on CRO oversight and study execution.

Responsibilities
  • manage clinical vendors, ensure trial compliance with GCP/ICH/FDA regulations, develop and review study documentation, conduct site visits, oversee investigational product reconciliation, and lead clinical trial teams.
Requirements
  • BS/MS with 5+ years in clinical operations
  • industry experience in early-phase oncology trials
  • strong knowledge of FDA, ICH, GCP guidelines
  • vendor management skills
Preferred
  • experience with cooperative group studies, investigator-sponsored trials, and global/regional (APAC) clinical trial operations.
High Value
  • oncology, Phase I-III, FDA/GCP compliance, vendor management, international trial oversight, ~25% travel.
Work Setup

onsite Redwood City, CA.

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