Integrated Evidence Generation (IEP/RWE/Epi) Lead
PfizerAbout the role
ROLE SUMMARY
The leader in this role will provide strategic leadership and drive innovation in medical study orchestration and design, including integrated evidence planning, research design, and implementation to ensure end-to-end evidence generation activities are strategically aligned, methodologically rigorous, and operationally efficient by harmonizing study design and delivery approaches, thereby strengthening the organization’s ability to support regulatory, clinical, payer, and patient-centered decision-making globally.
ROLE RESPONSIBILITIES
- Oversee cross-functional teams specializing in Integrated Evidence Planning (IEP), RWE/epidemiology study design, patient-centered research design and execution, and RWE/epidemiology methods development and innovation
- Set strategic direction for study design and orchestration, ensuring alignment with portfolio and therapeutic area objectives
- Drive innovation in methodologies including pragmatic trials, hybrid designs, synthetic controls, RWE/epidemiology methods, and patient-centered approaches
- Foster cross-functional collaboration among epidemiology, therapeutic area, and RWE innovation teams, as well as other internal and external stakeholders
- Partner across Medical, Clinical, Regulatory, Market Access/HEOR, Digital, and Commercial functions to deliver integrated evidence strategies
- Communicate effectively with senior leadership and key stakeholders to facilitate decision-making and alignment
- Ensure cost-effective evidence optimization across multiple internal and external stakeholders to demonstrate comparative effectiveness, safety, and value of Pfizer's medicines and vaccines
- Apply data, technology and advanced analytics such as AI to improve quality and economics of study design and orchestration
- Drive performance on metrics including R&D efficiency, effectiveness and equity
- Serve as an enterprise thought leader to internal stakeholders and external partners, shaping industry standards for evidence generation
- Lead resource stewardship, risk management, and capability building to ensure sustainable and scalable impact
- Define and track key metrics to measure success and drive continuous improvement
QUALIFICATIONS
- Advanced degree required: Master’s/MPH, PhD in Epidemiology or a related discipline, or MD.
- 15+ years of experience in clinical research or evidence generation within pharma or biotech, including 5+ years leading study design or protocol development
- Expertise in both traditional clinical trials and RWE methodologies
- Experience with decentralized, hybrid, and pragmatic trials strongly preferred
- Deep understanding of global regulatory and ethical requirements for clinical and non-interventional studies
- Proven track record of cross-functional leadership and in a highly matrixed environment and communicating effectively with senior leadership and key stakeholders to facilitate decision-making and alignment
ORGANIZATIONAL RELATIONSHIPS
- Member of Medical Evidence Development Leadership team
- Partners with leadership across Medical, Clinical, Regulatory, Market Access/HEOR, Digital and Commercial
Other Job Details:
- Posting end date: November 7, 2025
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 provider’s n
Apply for this role
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.
Apply Now →Generate Application KitFree account required — sign up in 30s