Associate Director US Medical Affairs, Patient Access and Quality of Care (PAQ) – Oncology

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.Job Description The Associate Director US Medical Affairs, Patient Access and Quality of Care (PAQ) – Oncology will have responsibility for leading the development of Medical Affairs (MA) strategies and Plans of Action (POA) within a component of the Oncology Therapeutic Area (TA) for US payers and key accounts. This position will report to the Sr. Director, Strategy Lead of PAQ Oncology. The Associate Director Medical Affairs – PAQ Oncology will support the US launch planning and execution for novel pipeline products, as well as other products in the oncology portfolio.Job Responsibilities (including, but are not limited to)In collaboration with global and USMA TA, Managed Markets, Value and Access, Commercial and Government Affairs, develop Medical Affairs strategies and POA to ensure that PAQ is improving patient lives by aligning patient population needs, external stakeholder value drivers and Gilead portfolio and products. He/She will provide frequent internal and external input into the development of the US PAQ Strategic Plans as well as the Integrated Evidence Plan.Identify and develop patient access strategy and research opportunities for US payers and key accounts ensuring alignment and inclusion of assigned MA activities, to support MA scientific objectives.Act as scientific and execution lead for local US oncology PAQ studies and projectsUnderstand PAQ OL needs, identify and communicate data gaps, and work collaboratively with research teams (Clinical Development, Medical Affairs Research, Value and Access Health Economic and Outcomes Research, Real-World Evidence) to actively address evidence needs throughout product lifecycle. Accountable for providing PAQ strategic input into Publication Strategy.Consistent with the scientific strategy, develop tools and resources to support successful implementation of the POA.Work effectively with external vendor partners to complete required tools and resourcesAnticipate and coordinate necessary knowledge development for the PAQ team, ensure continuous and timely resources and training are provided to facilitate PAQ field team scientific knowledge and exchangeProactively share insights and evidence needs with the PAQ Strategy LeadIn collaboration with PAQ field and cross-functional partners, contributes to strategy for real-world collaborative projects or studies and drives alignment with prioritized evidence needs / gapsLead communication strategy with PAQ stakeholders, including leveraging the appropriate avenues for early scientific engagement and AMCP and preapproval dossier development.In partnership with the FD’s, coordinate efforts for key PAQ conferencesAssist with management of PAQ Medical Affairs Advisory Programs (MAAPs)Develop and maintain positive professional relationships with PAQ thought leaders based on mutual respect and the sincere interest in sharing their perspective on medical therapies.May be responsible for preparing and giving presentations for internal training and/or external audiencesCollaborates effectively and in a compliant manner with colleagues in other functional areas throughout Gilead.Minimum Required Education and Years of ExperienceBachelor's Degree and Ten Years’ Experience ORMasters' Degree and Eight Years’ Experience ORPhD and Two Years’ ExperiencePreferred Education, Experience and Qualifications 4+ years Medical Affairs (medical device/pharmaceutical industry), managed care, and HEOR experience, required. Ideally including recent experience of a successful launch.Demonstrated experience and expertise in health economics and outcomes research including writing research protocols, partnering to execute observational and economic research, and leveraging study design to support appropriate messages for strategic needs.Advanced degree in life sciences in one or more of the following: MD, DO, PharmD, PhDSignificant health outcomes, research or medical affairs background in oncologyExcellent strategic thinking skills, with demonstrated ability to successfully lead the ideation, development of a plan and move to actionPossess a willingness and ability to work hands-on and with a sense of urgency, in a fast-paced, scientific, entrepreneurial environmentExtensive knowledge of the US healthcare ecosystems, payer landscape and payer evidence requirementsExisting contacts with payers, providers, advocates, institutions and/or hospitals strongly preferredSolid working knowledge of regulatory and compliance environmentEffective organizational, project planning, and time management skills. Strong sense of urgency and goal orientationProfessional written and verbal communication skills with the ability to effectively present to and engage with a wide range of audiencesStrong interpersonal skills including excellent verbal and written communicationProven ability for organizational partnersh