Revolution Medicines

Manager, Clinical Biomarker Operations

Revolution Medicines • $143K — $178K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Life sciences degree (BS or MS) in scientific, medical, healthcare, or related discipline.
  • 7+ years of professional experience in clinical research or clinical/diagnostic laboratory settings.
  • Experience mentoring team members is essential.
  • Strong preference for prior experience in clinical biomarker and CDx operations for phases I-III trials.
  • Familiarity with TruTech, SLOPE, and LIMS platforms is highly desirable.
  • Excellent communication and collaboration skills, with strong planning abilities.
  • Proficiency in Microsoft Excel and PowerPoint; experience with project management tools is a plus.

Responsibilities

  • Lead end-to-end biomarker operations for Phase I-III oncology clinical trials.
  • Collaborate with cross-functional teams on protocol and documentation reviews.
  • Oversee central lab activities, including lab startup and budget evaluations.
  • Manage relationships with specialty biomarker labs and oversee sample logistics.
  • Contribute to SOP development and operational process optimization.
  • Support TM deliverables, including data reviews and regulatory submissions.
  • Drive vendor selection and ensure compliance with regulatory standards.

Benefits

  • Robust equity awards and competitive cash compensation.
  • Strong benefits package including health and wellness programs.
  • Significant learning and development opportunities.
  • Commitment to inclusiveness and fairness in the workplace.
Full Job Description
The Opportunity:

Playing a critical role as a Manager, Biospecimen Operations within Translational Medicine function, the position will be providing biomarker operational expertise in, developing scope of work, and maintaining effective working relationships with cross-functional teams for phase three clinical trials.
  • 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 cross-functionally with Biomarker Leads, Companion Diagnostics, Clinical Operations, and Data Management on reviews of protocol, ICF, eCRF, DTS, Genomic Verification Forms, and eTMF documentation to ensure operational alignment.
  • Oversee central lab activities, including operational lab startup, lab manual and site requisition form, SOW reviews and budget evaluation.
  • Manage relationships with specialty biomarker labs, including sample logistics oversight, testing strategy alignment, RUO data transfer execution, issue and query resolution, invoice review, and coordination of recurring operational meetings.
  • Contribute to SOP development, operational process optimization, and biomarker program initiatives to support biomarker operation excellence.
  • Support TM deliverables, including IA data reviews, CSR, and regulatory submissions for CDx filings.
  • Drive vendor selection, qualification, 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 to support strategic decision-making.
  • Review ICFs and respond to EC and IRB inquiries related to biomarker components.
  • Bring experience in diagnostic operations supporting CDx development and regulatory filings, including sPMA submissions.
  • Utilize IRT and EDC systems to enable real-time sample tracking, data integration, and prompt query resolution.

Required Skills, Experience and Education:
  • Life sciences degree (BS or MS) in scientific, medical, healthcare, or related discipline.
  • 7+ years related professional experience in a clinical research setting, clinical/diagnostic laboratory.
  • Should have experience mentoring team members.
  • Prior experience in clinical biomarker and CDx operations in phase one to three clinical trials is strongly preferred.
  • Prior experience in TruTech, SLOPE and LIMS platforms is highly desirable.
  • Excellent scientific and business communication skills, strong interpersonal/collaboration skills, and planning skills.
  • Should be proficient in Microsoft Excel, Microsoft PowerPoint applications.
  • Experience in using Project Management tools is highly desired.
  • Ability to think critically and creatively and be able to work independently to determine appropriate resources for resolution of problems.
  • Ability to multi-task and thrive in a fast-paced innovative environment.
  • A great teammate, who listens effectively and invites response and discussion.
  • Commitment to Revolution Medicines' Core Values: Tireless Commitment to Patients, Transformative Science, Exceptional Together, Total Integrity, Inclusiveness and Fairness.

Preferred Skills:
  • Should be proficient in Microsoft Excel, Microsoft PowerPoint applications.
  • Experience in using Project Management tools is desirable.
  • Experience in using LIMS Sample Management tool is desirable.
  • Experience with next-generation sequencing (NGS) methods for RAS mutation analysis is desirable.

#LI-EM1 #LI-Hybrid

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

Base Pay Salary Range

$143,000-$178,000 USD

We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.

Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.

If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to [email protected] so we can share these impersonations with our IT team for tracking and awareness.

About Revolution Medicines

Revolution Medicines is a clinical-stage precision oncology company focused on developing targeted therapies to inhibit elusive frontier targets within notorious growth and survival pathways, with particular emphasis on RAS and mTOR signaling pathways. The company's proprietary platform enables the discovery and development of small molecules that bind covalently to proteins. Revolution Medicines was founded in 2014 and is headquartered in South San Francisco, California.
Learn more about Revolution Medicines
Size
201 employees
Market Cap
$2.1 billion
Industry
Net Income
-$108.1 million
Revenue
$42.9 million
NASDAQ

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