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Revolution Medicines

Clinical-stage oncology company developing RAS inhibitors

Manager – Clinical Biomarker Operations

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRedwood City, CA, USAIn-person

About the Job

Requirements

  • A Bachelor of Science or Master of Science degree in a scientific, medical, healthcare, or related discipline.
  • At least 7 years of related professional experience in a clinical research setting or clinical/diagnostic laboratory.
  • Experience mentoring team members.
  • Excellent scientific and business communication skills, interpersonal and collaboration skills, and planning skills.
  • Proficiency in Microsoft Excel and Microsoft PowerPoint.
  • Ability to think critically and creatively, work independently, and determine appropriate resources to resolve problems.
  • Ability to multitask and work effectively in a fast-paced, innovative environment.
  • Commitment to Revolution Medicines’ Core Values: Tireless Commitment to Patients, Transformative Science, Exceptional Together, Total Integrity, Inclusiveness and Fairness.

Responsibilities

  • Lead end-to-end biomarker operations across Phase I–III oncology clinical trials, including protocol reviews, prospective testing strategies, sample lifecycle oversight, data management, query resolution, and vendor qualification and contracting.
  • Collaborate with Biomarker Leads, Companion Diagnostics, Clinical Operations, and Data Management to review protocols, ICFs, eCRFs, DTS, Genomic Verification Forms, and eTMF documentation and ensure operational alignment.
  • Oversee central lab activities, including operational lab startup, lab manuals, site requisition forms, SOW reviews, and budget evaluation.
  • Manage relationships with specialty biomarker labs, including sample logistics, testing strategy alignment, RUO data transfer execution, issue and query resolution, invoice review, and recurring operational meetings.
  • Contribute to SOP development, operational process optimization, and biomarker program initiatives.
  • Support Translational Medicine deliverables, including IA data reviews, CSR, and regulatory submissions for CDx filings.
  • Drive vendor selection, qualification, and onboarding, and participate in audits to ensure adherence to regulatory and quality standards.
  • Provide biomarker operational metrics and study updates to cross-functional teams and senior leadership.
  • Review ICFs and respond to EC and IRB inquiries related to biomarker components.
  • Support diagnostic operations for CDx development and regulatory filings, including sPMA submissions.
  • Use IRT and EDC systems for real-time sample tracking, data integration, and query resolution.

Desired Qualifications

  • Prior experience in clinical biomarker and CDx operations in Phase I–III clinical trials is strongly preferred.
  • Prior experience with TruTech, SLOPE, and LIMS platforms is highly desirable.
  • Experience using project management tools is desired.
  • Experience using an LIMS sample management tool is desirable.
  • Experience with next-generation sequencing methods for RAS mutation analysis is desirable.

About the Company

Revolution Medicines

Clinical-stage oncology company developing RAS inhibitors

Revolution Medicines develops precision oncology drugs focused on cancers driven by RAS mutations. Its RAS(ON) inhibitors are small molecules that bind the active form of RAS to block cancer signaling, with candidates like Daraxonrasib (RMC-6236), Elironrasib (RMC-6291), and Zoldonrasib (RMC-9805) advancing in global Phase 3 trials. The company funds its research through collaborations, royalties, and upfront funding, and has not yet marketed a product. Its goal is to bring effective RAS-targeted therapies to patients and advance multiple candidates through late-stage trials toward approval, supported by strong cash reserves.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Redwood City, CA
Founded
2014

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