Full-Time Clinical Science Liaison (Central Territory)

The Clinical Science Liaison, Oncology provides scientific and technical leadership educating community-based physicians on the latest study findings (abstracts and publications), highlighting the clinical value of Guardant Health's product(s).

The role covers Missouri and Tennessee states.

Essential Duties and Responsibilities:

• Provide scientific and technical leadership for professional and credible relationships with key community physicians and KOLs to promote adoption of novel diagnostic technologies.
• Serve as a resource for community physicians evaluating and guiding interpretation of real-world patient test reports.
• Facilitate educational growth through presentations of scientific content to medical providers and staff.
• Identify opportunities for collaboration with KOLs to present at scientific forums (national/regional specialty society meetings).
• Summarize and educate key staff on emerging abstracts/publications relevant to molecular testing.
• Facilitate medical and scientific field intelligence (e.g., provider/investigator lists in specific tumor types).
• Gather feedback on current and future products for internal commercial and research divisions.
• Understand competitive research activities in active/planned study sites, and generate insights from investigators regarding sponsored clinical trial challenges/opportunities (communicate insights to Guardant).
• Prepare and present clinical requests for information related to institutional guidelines/pathways.

Requirements:

• Terminal degree (Genetic Counselor, NP/PA, Pharm.D., Ph.D., M.D. or academic equivalent).
• Clinical expertise/experience in Oncology.
• 1-3 years of healthcare experience (pharmaceutical/biotech industry).
• Experience working with clinicians to build consensus around new products/services.
• Track record of independent presentations at major academic centers/community resulting in product adoption.
• Prior experience introducing a novel clinical product (highly desired).

Skills:

• Advanced knowledge of biotechnology, diagnostics, pharmaceutical industry.
• Proficiency in Excel, Word, PowerPoint, and other software.
• Excellent written/verbal communication skills.
• Ability to work independently and remotely.
• Strong teamwork ethic.
• Multi-tasking abilities to work on simultaneous tasks, cross-teams, and at different levels (internal/external).
• Self-directed, flexible in dynamic environment.
• Strong problem-solving, attention to detail, time management, and initiative.
• Excellent human relations to coordinate tasks through others.
• Ability to elicit and answer clinical questions in various settings (individuals to roundtables).

Work Environment:

• Extensive travel required (up to 3-4 days/overnights per week).
• Home-based office with computer/keyboard use.
• Potential exposure to high noise levels, fumes, biohazard material (laboratory).
• Ability to sit for extended periods.

Salary: $136,585 - $184,400 (USD). Includes base salary, does not include benefits, bonus, commissions, or equity.

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