Associate Director, Portfolio Program Management

Company DescriptionGuardant 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. The Associate Director, Program Manager for new product development is a key leadership role on the team. Your primary responsibility will be to lead a complex, multi-disciplinary core team to launch products for Research Use Only (RUO), Lab Develop Tests (LDT), and In Vitro Diagnostics (IVD) that meet critical unmet needs for cancer patients. You will lead a cross functional core team in the development of a NGS assays, automation, and infrastructure, ensuring delivery of the product through launch while ensuring compliance with Guardant Health’s quality system deliverables and regulatory requirements. Experience with IVD or Medical Device product development will be critical to the success of this role. Successful end-to-end product development with complex systems is a must.You will work closely with key stakeholders across the organization, including marketing, regulatory, quality, medical affairs, reagent development and bioinformatics teams, among others. In addition, you will lead the joint project team with our external partners.Essential Duties and Responsibilities:Lead a cross functional product development core team in the execution of deliverables. Work closely with R&D, Operations, Quality, Marketing, Regulatory, Medical Affairs and other departments to ensure project priorities and decisions are consistent between teams and corporate strategic plansLead a cross functional joint project team with external partners to align and execute the project per contractual milestonesCommunicate program updates to the core team, to functional management and to executive leadership both internally and externallyEnsure timely team completion of documents required for the product design history fileLead team efforts to mitigate risks and resolve issues quickly as they ariseLead the team through problem resolution including root cause analysis and corrective actionLead the team to prepare for phase gate reviews and other go/no go decisions required by executive leadershipLead the program planning, monitoring, and reportingEnsure effective communications with the Core Teams using a variety of tools and channelsDefine program resource needs, negotiate program resourcing plans and track resource usage over the course of the programPerform other related duties and assignments as requiredManage leadership stakeholders and present at executive management forumsQualifications:Bachelors degree in a business or a technical discipline. An advanced degree in either business or a technical field is desired. Relevant experience of 5 to 8 years with BS/BA and 3-5 years with Masters degree in addition to meeting the experience requirementsPMP or similar certification is highly desiredExperience working in team environments is required.Expert level knowledge of Program / Project Management tools such as project scheduling, work breakdown structures, time and cost reporting is required.Experience working in FDA-regulated environments is requiredExperience leading core teams to successfully launch medical devices or in vitro diagnostic products is highly desiredSpecific experience managing complex system programs with multiple sub projects as part of a complete solution is requiredExperience in product development for NGS assays is desiredPosition requires the ability to collect information from multiple sources, sort through, integrate, and resolve often conflicting requirements, and drive an organization through the various issues to result in a successful product launchExperience with both Agile and Waterfall program management is requiredAI & Digital FluencyDemonstrate curiosity, sound judgment, and the ability to critically evaluate and responsibly leverage AI-enabled tools in accordance with company policies, ethical standards, and regulatory requirements to improve the efficiency, effectiveness, and quality of work.Hybrid Work Model:This section is applicable to onsite employees who are eligible for hybrid work location as specified by management and related policies. Guardant has 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 annualized base salary ranges for the primary location and any additional locations are listed below. This range does not include benefits or, if applicable, bonus, commission, or equity. Each candidate’s compensation offer will be based on multiple factors including, but not limited to, geography, experience, education, job-related skills, job duties, and business need. Primary Location: Palo Alto, CA Primary Location Base Pay Range: $199,400 - $274,200 Other US Location(s) Base Pay Range: $169,490 - $233,070 If the role is performed in Colorado, the pay range for this job is: $179,460 - $246,780Employee 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 View email address on us.fitly.work background screening including criminal history is required for this role. GH will consider qualified applicants with criminal arrest or conviction histories in a manner consistent with applicable law including but not limited to the LA County Fair Chance Policies and the Fair Chance Act (Gov. Code Section 12952).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: SummaryLocation: Palo Alto, CAType: Full time