Senior Director

Guardant Health is a leading precision oncology company focused on helping conquer cancer globally through use of its proprietary tests, vast data sets and advanced analytics. The Guardant Health oncology platform leverages capabilities to drive commercial adoption, improve patient clinical outcomes and lower healthcare costs across all stages of the cancer care continuum. Guardant Health has commercially launched Guardant360, Guardant360 CDx, Guardant360 TissueNext, Guardant360 Response, and GuardantOMNI tests for advanced stage cancer patients, and Guardant Reveal for early-stage cancer patients. The Guardant Health screening portfolio, including the Shield test, aims to address the needs of individuals eligible for cancer screening. The Senior Director, Medical Strategy Medical Affairs, Oncology is a key leadership position responsible for guiding the medical strategy and overseeing the execution of medical affairs activities within the oncology portfolio. The Senior Director, Medical Strategy Medical Affairs, Oncology represents US Medical Affairs, Oncology and works closely with commercial and product leadership in cross-functional core teams to drive business objectives. The Senior Director, Medical Strategy Medical Affairs, Oncology involves managing clinical and scientific projects and establishing strong relationships with key stakeholders in the oncology community. The ideal candidate will have extensive experience in oncology, a strategic mindset, and a proven track record of leadership in Medical Affairs. Key Responsibilities Works closely with marketing and product leadership in cross-functional commercial core teams and provides medical and scientific input into marketing strategies, promotional materials and programs. Align medical affairs initiatives with the overall corporate objectives and business strategies. Identify and evaluate new scientific opportunities and trends to enhance the oncology portfolio. Monitor and communicate on clinical molecular genomics competitive landscape and new technology. Develop and implement comprehensive medical affairs strategies that support the oncology portfolio. Lead the development, execution, and annual update of the Medical Affairs Strategic Plan for disease areas and/or oncology products including the pre-launch and product launch plans, Develop the data and product scientific narrative in collaboration with USMA, marketing and product leadership Train and distribute scientific narrative ensuring consistent aligned external positioning and messaging. Collaborate with tech development, regulatory, commercial, and marketing teams to align medical strategies with business goals. Build and maintain strong relationships with key opinion leaders (KOLs), healthcare professionals, and other stakeholders in the oncology field. Represent the company at scientific conferences, advisory boards, and other external meetings. Collaborate with patient advocacy groups and professional societies to support awareness and education initiatives. Use expert opinion leader feedback to influence medical strategy, publication strategy, commercial strategy, and product development strategy. Deliver high-quality medical education programs and materials for internal and external audiences. Ensure accurate, timely, and compliant communication of scientific data and product information. Support medical/scientific writing, document editing, and review manuscript review for consistent messaging. Ensure all medical affairs activities comply with regulatory requirements and company policies. Develop and maintain standard operating procedures (SOPs) and training programs for the Medical Affairs team. Monitor the medical environment to ensure compliance with relevant guidelines and standards. Lead, mentor, and develop a high-performing Medical Affairs team. Foster a culture of scientific excellence, collaboration, and continuous improvement. Manage the Medical Affairs budget and resources effectively. MD, PhD, or other advanced clinical degree with relevant medical training required. 10+ years of Medical Affairs experience or related pharmaceutical industry experience in oncology genomic diagnostics. with at least 5 years in a senior leadership Knowledge in oncology therapeutic area, functional genomics, and molecular biology. Proven track record of developing and executing successful medical strategies. Extensive experience in clinical research, regulatory interactions, and scientific communication. Proficiency in medical strategy, clinical development, and field medical activities. Ability to independently develop and deliver strategic plans and medical initiatives/projects. Exceptional written and verbal communication skills with the ability to convey complex scientific information clearly. Strong analytical and problem-solving skills. Excellent external and internal communication and relationship-building skills. Ability to work effectively in a cross-functional team environment focused on successful outcomes. Ability to travel up to 60% of the time. Superior attention to detail with the ability to find and correct errors in spelling, punctuation, grammar, consistency, clarity, and accuracy 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. The US base salary range for this full-time position is $272,000 to $367,200. 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). 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 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. To learn more about the information collected when you apply for a position at Guardant Health, Inc. and how it is used, please review our Privacy Notice for Job Applicants. Please visit our career page at: