Job Description

Guardant Health is a leading precision oncology company focused on guarding wellness and giving every person more time free from cancer. Founded in 2012, Guardant is transforming patient care and accelerating new cancer therapies by providing critical insights into what drives disease through its advanced blood and tissue tests, real-world data and AI analytics. Guardant tests help improve outcomes across all stages of care, including screening to find cancer early, monitoring for recurrence in early-stage cancer, and treatment selection for patients with advanced cancer. For more information, visit  guardanthealth.com and follow the company on  LinkedIn ,  X (Twitter)and  Facebook .

Job Description

This role will report to the Senior Director of Publications within Medical Affairs and will support the Real-World Data/Evidence (RWD/E) activities of Guardant Health. The ideal candidate will have a strong background in analyzing both quantitative and qualitative data, and will be responsible for generating insights and evidence analytics across various domains – including observational research, reimbursement and payer evidence generation, clinical development, key opinion leaders (KOL) research requests related to oncology diagnostics, and contribute in the development of scientific publications.

Essential Duties and Responsibilities:

• Design, develop, oversee and execute RWE studies in support of clinical utility, health outcomes and economic value across all Guardant Health oncology diagnostics products, in collaboration with the Medical Affairs field team, cross-functional partners, and external key opinion leaders (KOLs)
• Collaborate closely with cross-functional teams to align real-world data/evidence (RWD/E) strategies and data visualizatoin, translating scientific and clinical needs into actionable insights and ensuring the delivery of high-impact analytics and outcomes
• Independently develop, validate and execute statistical programs within standard statistical software packages such as R, python, SAS and advanced analytics methods, and prepare materials for presentation to internal and external specialist and generalist audiences
• Present study results and communicate complex data in a clear, compelling way to external stakeholders including KOLs, academic collaborators, internal collaborators and policy-makers
• Partner with internal and external KOLs in developing scientific publications including conferences abstracts, posters for scientific conferences and peer-reviewed manuscripts and white papers

Qualifications

• Experience in oncology, diagnostics field, or precision medicine is a strong plus
• Experience in designing and deploying advanced analytical techniques and algorithms to derive insights from internal and external healthcare data sources
• Advanced degree (Masters, PhD) in relevant field of study (outcomes research, epidemiology, statistics, advanced data science and/or analytics, mathematics or other relevant) is required
• 8+ years of relevant experience in health related outcomes research in the pharmaceutical or biotechnology or device environment
• Strong proficiency in R (preferred), Python, or SAS, including hands-on experience writing statistical programs

• Demonstrated ability to work in teams in a highly matrixed environment
• Extensive experience in real-world data analytics, observational research study design, execution and outcome research studies
• Able to adapt to novel methodological approaches to outcomes research in a rapidly advancing field of study
• Excellent written and verbal communication skills; ability to clearly articulate and synthesize evidence to both technical and non-technical audiences

Additional Information

Hybrid Work Model : At Guardant Health, we have defined days for in-person/onsite collaboration and work-from-home days for individual-focused time. All U.S. employees who live within 50 miles of a Guardant facility will be required to be onsite on Mondays, Tuesdays, and Thursdays. We have found aligning our scheduled in-office days allows our teams to do the best work and creates the focused thinking time our innovative work requires. At Guardant, our work model has created flexibility for better work-life balance while keeping teams connected to advance our science for our patients.

*pay transparency*

For positions based in Palo Alto, CA or Redwood City, CA, the base salary range for this full-time position is $144,200 to $198,250. The range does not include benefits, and if applicable, bonus, commission, or equity.

The US base salary range for this full-time position is $144,200 to $198,250. The range does not include benefits, and if applicable, bonus, commission, or equity.  The range displayed reflects the minimum and maximum target for new hire salaries across all US locations for the posted role with the exception of any locations specifically referenced below (if any).

Within the range, individual pay is determined by work location and additional factors, including, but not limited to, job-related skills, experience, and relevant education or training. If you are selected to move forward, the recruiting team will provide details specific to the factors above.

Employee may be required to lift routine office supplies and use office equipment. Majority of the work is performed in a desk/office environment; however, there may be exposure to high noise levels, fumes, and biohazard material in the laboratory environment. Ability to sit for extended periods of time.

Guardant Health is committed to providing reasonable accommodations in our hiring processes for candidates with disabilities, long-term conditions, mental health conditions, or sincerely held religious beliefs. If you need support, please reach out to  Peopleteam@guardanthealth.com

Guardant Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

All your information will be kept confidential according to EEO guidelines.

Please visit our career page at: 

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