G

Guardant Health

FDA-approved blood-based cancer diagnostics provider

Medical Science Liaison - Oncology

Biology & BiotechUpdated on Nov 14
Full-timeMissouri, USA$145k - $199.3k /yr

About the Job

Requirements

  • Clinical expertise or related experience in oncology is required.
  • A university degree and typically five years of related experience, a master's degree and three years of related experience, or a PhD is required; terminal degrees in a scientific field of study, including Genetic Counselor, NP/PA, Pharm.D., Ph.D., M.D., or academic equivalent such as an Associate Professor position, are also accepted.
  • Experience working with clinicians to build consensus around new products or services is required.
  • A track record of independent presentations at major academic centers or in a community setting resulting in product adoption is required.
  • Advanced knowledge of the biotechnology, diagnostics, and pharmaceutical industries is required.
  • Proficiency in Excel, Word, PowerPoint, and other software is required.
  • Ability to work independently and remotely while maintaining a strong teamwork ethic is required.
  • Ability to work on simultaneous tasks, across teams, and at different organizational levels with internal and external relationships is required.
  • Ability to elicit and answer clinical questions in groups ranging from individuals to larger didactic roundtables and meetings is required.
  • Ability to critically evaluate and responsibly leverage AI-enabled tools in accordance with company policies, ethical standards, and regulatory requirements is required.
  • Extensive travel of approximately 75%, including up to three to four days or overnights per week and occasional weekend work, is required.
  • Ability to sit for extended periods is required.

Responsibilities

  • Provide scientific and technical leadership to establish professional and credible relationships with key community physicians and key opinion leaders and promote understanding and adoption of the company's diagnostic technologies.
  • Help community physicians evaluate and interpret real-world patient test reports.
  • Present scientific content to medical providers and their staff to facilitate education and understanding.
  • Identify opportunities to collaborate with key opinion leaders on presentations at national and regional specialty society meetings and address other strategic industry medical needs.
  • Summarize and educate key staff on emerging abstracts and publications relevant to molecular testing.
  • Facilitate medical and scientific field intelligence, including identifying providers or investigators in specific tumor types; elicit feedback on current and future products and share it with commercial and research divisions; understand competitive research activities at active or planned study sites; generate investigator insights on challenges and opportunities for sponsored clinical trials; and communicate relevant information within the company.
  • Prepare and present clinical requests for information related to institutional guidelines or pathways.
  • Build relationships with local and regional professional societies and health plans to provide education on emerging abstracts and publications relevant to molecular testing as those entities develop policy.
  • Use AI-enabled tools responsibly to improve the efficiency, effectiveness, and quality of work, consistent with company policies, ethical standards, and regulatory requirements.

Desired Qualifications

  • Prior experience introducing a novel clinical product is highly desired.

About the Company

Guardant Health

FDA-approved blood-based cancer diagnostics provider

Guardant Health develops blood-based cancer diagnostics and sells tests to healthcare providers and research institutions. Its flagship product, Guardant360, uses a liquid biopsy to analyze tumor DNA circulating in a patient’s blood to detect mutations and guide treatment decisions for advanced cancer. The company is expanding into early detection and recurrence monitoring, with tests designed to be non-invasive and data-rich for cancer management. Compared with competitors, Guardant Health emphasizes a widely adopted, FDA-approved liquid biopsy platform with broad cancer-type coverage and a focus on providing actionable genomic insights to clinicians. Its goal is to improve cancer outcomes by enabling non-invasive, data-driven decision making across stages of disease and over time.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Palo Alto, CA
Founded
2012

Recently Posted Jobs

Explore more opportunities at Guardant Health

See more jobs