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Job Details

Job Title Director

JobID 1053264-1852

Location: New York, NY

Description *About Pfizer*

A career at Pfizer offers opportunity, ownership and impact.All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.

*Role Description*

To support the strategic goals of the Oncology Business by driving optimal patient access for our RCC and I/O medicines. This role directly impacts the ability to achieve business objectives on a global basis by providing strategic guidance and robust evidence development relevant to achieve optimal global patient access by demonstrating the value of our products. The O&E Director will be responsible for independently leading the evidence generation strategy at a Global level, including oversight and development of evidence generation and dissemination of technical deliverables that support the value of our Oncology RCC and I/O medicines. She/he will function with a one Patient and Health Impact (PHI) mindset and will work in a closely with the Payer Insights and Access (PI&A) and the Cross-Functional Leadership Team (CFLT) to ensure there is a single and coordinated view on strategy and delivery for PHI to the Oncology business. This position resides within the PHI O&E group, reporting to the Global O&E - Oncology/Immuno-Oncology Team Lead.


Lead the development of Outcomes and Evidence (O&E) strategy to support the value of assets in the Oncology Business Unit (BU) in close partnership with the cross-functional matrix team.Lead the execution of O&E studies and projects (including Non-Interventional Studies, registries, etc) in alignment with the global O&E strategy and demonstrate the value proposition for assets in the Oncology BU. Incorporate humanistic and economic endpoints into clinical trials across all phases of product development to build comprehensive trial-based evidence in line with overall medical strategy for the assets and to ensure global reimbursement and access requirements. Provide strategic input in the selection of relevant patient population and comparators within clinical trials to enable successful negotiations, reimbursement, and appropriate patient access with global payer and regulatory decision makers.Development and validation of new Patient Reported Outcomes measures as appropriate for inclusion across clinical trials, registries, and prospective real world studies.Identify opportunities to partner with Oncology BU external customers to conduct O&E projects in support of asset strategiesLead the timely development of launch and post launch deliverables including global value dossiers (GVDs), evidence blueprints, economic models, and innovative tools to successfully support global launch and post-launch reimbursement and access requirements in conjunction with the regions/countries.Lead the coordination of input from local country/regional teams on evidence needs and ensure that the input is appropriately incorporated to develop and integrated evidence strategy to support global market access needs at launch and through lifecycle.Develop real world evidence generation strategies and flawlessly execute studies (e.g., burden of illness studies, epidemiology studies, etc).Develop strategic partnerships and research collaborations with key external experts, healthcare policy makers, payers, and various academic and community oncology settings to support asset strategies. Provide strategic guidance and content guidance in reimbursement (re)negotiations for Pfizer products.Lead the development of appropriate data dissemination plans and communicate evidence generated via publications and conference presentations.


Minimum Master's degree (MSc, MPH) in health services research, public health, epidemiology, or health economics with a preferred Doctoral degree (PhD, DrPH, ScD) in health services research, public health, epidemiology, or health economics. Minimum 8 years' experience in health outcomes and related fields, 5 of which are as part of global health economics and/or outcomes research teams in a pharmaceutical company. Strong working knowledge of the technical and methodological aspects of registries and observational study design and implementation. Capable of independently managing complex registry and non-interventional study projects.Strong methodological skills (study design, data analysis and interpretation) in cancer epidemiology or health services research is requiredIn depth understanding of Pharmacoeconomics and Health-related Quality of LifeKnowledge and experience in the oncology therapeutic area is preferredExperience with HTA organizations such as NICE, SMC, PBAC is desirableExcellent interpersonal skills required: ability to understand and respond to multiple internal and external customersExcellent oral and written English communication skills requiredStrong project management abilities (contracting, budgeting, vendor management) essential. Demonstrated ability to manage multiple projects (multitask) involving complex processes, significant budget, competing deadlines and rapidly shifting prioritiesAbility to influence key members of medical and commercial teams constructively and without conflictSkilled in functioning within a matrix organization where managing through influence is requiredOrganized and detail oriented with the ability to anticipate needs and to work proactively to prioritize & address/resolve Change oriented, comfortable responding to unexpected demands with tight timelines; team player.Demonstrated expert understanding of fundamental health services research methods (e.g., health economics, patient reported outcomes, study design, database analyses, epidemiology, statistics)Able to independently engage all levels of internal and external stakeholders through strategic thinking, leading change, and building collaborative partnerships in a matrix environmentDemonstrated ability to manage multiple projects (multitask) involving complex processes, significant budget, competing deadlines and rapidly shifting prioritiesEstimated 10-20% International and US based travel will be required.

*EEO & Employment Eligibility*

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.

*New York, New York*

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