Revolution Medicines

Associate Director, Clinical Biomarker Development

Revolution Medicines$186K — $233K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. in cancer biology, cell/molecular biology, genomics or equivalent required
  • 3+ years of clinical biomarker and/or assay development experience in industry
  • Proven track record in development, validation, and implementation of biomarker readouts
  • Experience collaborating with Contract Research Organizations (CROs)
  • Excellent scientific and business communication skills
  • Strong interpersonal, collaboration, and planning skills
  • Ability to think critically, creatively, and work independently

Responsibilities

  • Develop and maintain biomarker strategies to support clinical trials from phase 1 to phase 3
  • Support trial design focusing on biomarker-related aspects, including assay development
  • Participate in clinical working groups and execution teams
  • Collaborate with internal and external partners to validate assays for clinical use
  • Manage outsourcing to CROs, overseeing contracts, budgets, and timelines
  • Work with Bioinformatics and Cancer Genomics on biomarker analysis and presentations

Benefits

  • Competitive cash compensation
  • Robust equity awards
  • Strong benefits package
  • Significant learning and development opportunities
  • Hybrid work model
Full Job Description
The Opportunity:

The Associate Director in Clinical Biomarker Development team, within Translational Medicine will play a key role in the design, execution, and interpretation of clinical biomarker strategies across Revolution Medicine's oncology pipeline. You will:
  • Develop and maintain translational and clinical biomarker strategies to support portfolio assets from phase 1 to phase 3 studies.
  • Support the development of biomarker related aspects of the trial design, including assay development, patient sample acquisition, study protocols, clinical biomarker plans, and other regulatory documents.
  • Participate in cross-functional teams such as clinical working groups and clinical study execution teams.
  • Work with internal translational groups, contract research organizations and collaborators to develop and validate assays for clinical use.
  • Manage outsourcing to CROs, oversee development of the scope of work, contracting, budgets, and timelines.
  • Collaborate with Clinical Bioinformatics and Cancer Genomics to support analysis of biomarker readouts, presenting outputs to internal and external stakeholders.

Required Skills, Experience and Education:
  • Ph.D in cancer biology, cell/molecular biology, genomics or equivalent is required.
  • 3+ years of clinical biomarker and/or assay development experience in industry is required.
  • Experience and track-record of the development, validation, and clinical implementation of biomarker readouts is required.
  • Experience of working with Contract Research Organizations to deliver biomarker readouts is required.
  • Excellent scientific and business communication skills, strong interpersonal/collaboration skills and planning skills.
  • 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.

Preferred Skills:
  • Experience with targeted oncology therapies or RAS/MAPK pathway biology.
  • Biological understanding of pancreatic, non-small cell lung and/or colorectal cancers is preferred.
  • Familiarity with biomarker platforms such as genomic, transcriptomic and proteomic assays.
  • Familiarity with analytical software and analytical capabilities for integrating clinical and biomarker datasets.

#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

$186,000-$233,000 USD

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

Similar Jobs

More Jobs at Revolution Medicines

More Pharmaceuticals & Biotech Jobs

Find similar Associate Director, Clinical Biomarker Development jobs: