Director, HTA, Value & Evidence (HV&E) - Lung Cancer
Director, HTA, Value & Evidence (HV&E) - Lung Cancer
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$ 169700 - 282900
1 Vacancy
Job Description
ROLE SUMMARY
As a leading biopharmaceutical company Pfizer is dedicated to the discovery and delivery of high value therapies across a variety of disease areas. It is our mission to bring innovative medicines to patients that significantly improve their lives and our priority is to ensure patients have access to these medicines.
The Health Technology Assessment (HTA) Value & Evidence (HV&E) team is responsible for ensuring patients have affordable timely access to medicines and vaccines by advancing innovative value and evidence solutions to inform healthcare decision-making.
The Director HTA Value & Evidence (HV&E) Lung Cancer will support the strategic goals of the Oncology Division by driving optimal patient access for Pfizers lung cancer portfolio.
This role influences global business objectives by guiding strategic evidence development to ensure optimal patient access for Lorbrena (lorlatinib). The HV&E Director will be responsible for developing and executing against the global evidence generation strategy including direct oversight of evidence generation activities and dissemination of technical deliverables.
This position will be part of Pfizers dynamic Global Access & Value (GAV) team and will have the important role of managing health economics and outcomes research (HEOR) to generate data to support patient access to position will be working closely with the broader Thoracic & Precision Medicine GAV team cross-functional (e.g. medical clinical commercial etc.) and country teams to foster a culture that promotes innovation and thrives on doing better for Pfizers patients and society in general.
ROLE RESPONSIBILITIES
- Lead the development of the evidence generation strategy to support the value of lung cancer assets as the lorlatinib global HV&E lead in close partnership with the cross-functional matrix team (e.g. medical commercial access strategy/pricing statistics clinical).
- Lead the coordination of input from local country/regional teams on evidence needs and ensure that the input is appropriately incorporated into the evidence strategy to support global market access needs at launch and through lifecycle.
- Lead the design and execution of global HEOR studies (e.g. network meta-analyses non-interventional studies economic models) from concept through publication.
- Lead the timely development of launch deliverables including value & evidence strategy global value dossiers/AMCP/JCA dossiers systematic literature reviews economic models and innovative tools to successfully support reimbursement and access requirements in partnership with the regions/countries.
- Develop patient-reported outcomes strategy and incorporate humanistic and economic endpoints into clinical trials across all phases of product development to build comprehensive trial-based evidence aligned with overall asset strategy and to ensure global reimbursement and access requirements.
- Provide strategic input into clinical trial designs (eg patient populations comparators endpoints) and analysis to enable successful negotiations reimbursement and appropriate patient access with global payer and regulatory decision makers.
- Partner with internal stakeholders to ensure appropriate customer facing dissemination of HEOR materials per regulatory guidance and internal SOPs.
- 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.
BASIC QUALIFICATIONS
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers develop and coach others oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
- Graduate degree required (e.g. MSc MPH PhD DrPH)
- 7 years of experience with MSc/MPH/MBA degree; 5 years with PharmD/PhD/DrPH in HEOR or relevant related fields (health economics epidemiology health services research or other research-focused public health field)
- Expertise in HEOR strategy evidence development fundamental health services research methods and tools including health economic modeling patient-reported outcomes statistics and real-world evidence studies including technical and methodological aspects of registries and observational study design implementation analysis and interpretation.
- Capable of independently managing complex non-interventional study projects
- Knowledge and understanding of drug development process
- Excellent interpersonal skills required: ability to understand and respond to multiple internal and external customers
- Excellent oral and written English communication skills
- Demonstrated ability to assess anticipated value for projects/programs to ensure alignment to business priorities and prioritize accordingly
- An execution mindset focused on getting things done quickly and simply
- Strong 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 priorities and expertise in stakeholder engagement
- Leadership in cross-functional teams (e.g. influence medical clinical and commercial teams constructively and without conflict); strategic thinking and ability to guide junior team members
- Skilled in functioning within a matrix organization
- Organized 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
PREFERRED QUALIFICATIONS
- Knowledge and experience in oncology or lung cancer
- Experience with HTA organizations such as NICE CADTH PBAC ICER and other HTA groups
- Knowledge of industry trends (e.g. IPAY EU HTA Regulation)
- Demonstrated publication history in venerable peer reviewed journals
- Experience in the biotech/pharmaceutical industry
- Experience in supporting a global oncology launch
- Experience leading retrospective cohort studies across various public and proprietary databases
- Experience in planning and executing a variety of real-world study designs (e.g. prospective/registries cross-sectional etc.)
- Ability to communicate technical and complex epidemiological and statistical concepts to various audiences
- Experience leveraging data from real-world to impact decision making
Other Job Details:
- Last Date to Apply for Job: July 21st 2025.
- Ability to travel based on business needs (25%)
- NOT eligible for Relocation Package
- This position is hybrid and requires working onsite 2 to 3 days per week
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care providers name address and the type of payments or other value received generally for public disclosure. Subject to further legal review and statutory or regulatory clarification which Pfizer intends to pursue reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse your name address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter please do not hesitate to contact your Talent Acquisition representative.
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. This position requires permanent work authorization in the United States.
Required Experience:
Director
Employment Type
Full-Time
