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 - We are seeking a highly motivated individual to join us as an Associate Director. Primarily, this position will be responsible for the development of ACE Health Economic and Outcomes Research (HEOR) strategies and tactical execution of YESCARTA launch indications and lifecycle management, managing HEOR projects from inception to completion for all phases of research. The role may also support other Kite indications such as Tecartus, anito-cel or pipeline.Your role will encompass research design, project management, analysis, interpretation and dissemination of HEOR evidence, and the communication of appropriate HEOR key value messages. You will collaborate cross-functionally with Clinical Development, Medical Affairs, Market Access, Government Affairs, Legal & Regulatory, and other Commercial functions, as well as collaborate with external KOLs and decision-makers. This position sits in the regional ACE HEOR team reporting to the ACE head of HEOR. The roles is based in Stockley Park, London (UK). Key responsibilities will include, but are not limited to, the following: - Supports the development of evidence to establish the clinical, economic, and patient centered value propositions related to YESCARTA launch indications and lifecycle management. - Supports the development of systematic literature reviews, meta-analysis, indirect treatment comparisons, real-world outcomes studies including registries and claims data, patient-reported outcomes (PRO) studies, cost-effectiveness and budget impact models, and other studies to support evidence generation for value prop and core value dossier - Manages budgets and timelines for vendor activities in support of our evidence generation activities - Interfaces with cross-functional partners in Medical Affairs, Clinical Development, Regulatory, Legal/Compliance, and Commercial in the development of HEOR strategy and evidence generation - Represents Kite for HEOR-related activities at external professional, scientific meetings and forums - Collaborates with internal and external experts in the execution of studies and implementation of field-based, customer-focused initiatives (e.g., models, scientific communications, slide kits, formulary/regulatory dossiers) - Provides internal training on HEOR methodologies and data results to key internal colleagues - Works closely with scientific communications, publications and other home office and field colleagues to ensure scientific conference material is appropriate, relevant and accurate - Creates study concept documents, protocols, analysis plans, and final study reports, as well as draft manuscripts for studies which include HEOR components - Develops health economic analyses and/or economic models to assess cost-effectiveness, clinical practice, and/or burden of illness within Kite's clinical trial design and study results, or external databases, or from scientific literature - Works with Medical Affairs to help influence Phase IV clinical trial design, inclusion of appropriate value endpoints/metrics, data analysis and publications, as appropriate. Manage external HEOR consulting companies Basic Qualifications: - MA/MS and extensive experience OR - BA/BS and extensive experience Preferred Qualifications: Experience - Advanced degree in the life sciences (PharmD, PhD, MD) or dual degree in related scientific field; will also consider a MS in an outcomes-related field (e.g., Public Health, Epidemiology, Health Economics, and Pharmacy Administration), a PharmD with HEOR-related education and/or Fellowship experience, or an MPH/MS who has strong relevant experience - Extensive experience in the industry, specifically in health economics and outcomes research, with clinical background or research experience necessary to support European, Canadian and Australian Market Access - Presentation and strong research experience with Market Access customers - Prior corporate experience in hematology/oncology therapeutic area is highly preferred - Experience with economic modeling and/or patient reported outcomes (PROs) is preferred - Experience with clinical/outcomes research applied to retrospective and prospective HEOR research - Experience influencing strategy with internal and external customer audiences - Significant experience in analyzing claims databases and EMRs to assess the burden of disease Skills/Knowledge - Superior technical reading, writing and verbal communication skills with proficiency in communicating clinical technical information to varied internal and customer audiences - Strong research design, modeling, and analytic skills - Refined methodological, quantitative and analytical skills - Strong track record in HEOR study methodology, statistics, data reporting and resource development - Demonstrated ability to manage a large number of complex projects - High level strategic thinking, critical thinking, problem solving and decision-making skills - Strong presentation and leadership skills - Highly motivated to function proactively, operate with a sense of urgency, bring tasks to completion - Ability to work independently with minimal supervision and collaboratively as a key contributor to multi-departmental teams simultaneously Equal Employment Opportunity (EEO) It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual's gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws. For Current Gilead Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday. Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.