Medical Evidence Generation Systems Lead
PfizerAbout the role
ROLE SUMMARY
The Medical Evidence Generation Systems Lead is accountable for the end-to-end ecosystem of digital tools that enable Medical Evidence study ideation, design, and execution across Pfizer’s Evidence Generation (EvGen) landscape.
Leads strategy, integration, and continuous improvement for the connected suite of systems – including the RISE Platform, IEP Portal, Portfolio Management, Study Design & Approval, and Study Management Systems.
Oversees seamless interoperability with Resource Management and Financial Management systems to ensure unified data flow, visibility, and governance from concept through delivery.
Partners with stakeholders across Medical Affairs, R&D, Digital, and Operations to modernize the MED technology backbone, enhance study efficiency, and enable evidence planning, execution, and reporting through simplified, connected, and compliant digital experiences.
ROLE RESPONSIBILITIES
Define and execute the EvGen systems roadmap aligned to business and compliance priorities
Integrate platforms across portfolio, study, resource, and financial systems to enable end-to-end data flow.
Drive innovation through digital transformation, automation, and advanced analytics.
Establish governance, KPIs, and continuous improvement frameworks for system performance and adoption.
Collaborate with Digital and build strong partnerships with Medical Affairs, R&D, and enabling functions to align systems with business needs.
Lead cross-functional and vendor teams delivering high-quality, user-focused solutions.
BASIC QUALIFICATTIONS
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.
Advanced degree (MS, MBA, PharmD, or equivalent) in Information Systems, Life Sciences, or related field.
10+ years leading enterprise platforms, systems integration, or digital transformation in global pharma or R&D.
Proven experience managing complex, cross-functional technology programs spanning study planning and operations.
Strong knowledge of evidence generation processes, governance, and compliance.
PREFERRED QUALIFICATTIONS
Experience managing Salesforce-based or equivalent workflow platforms for study or portfolio management.
Familiarity with GxP environments, validation standards, and data privacy and security requirements.
OTHER JOB DETAILS:
Last Date to Apply for Job: December 15th, 2025
This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week or more as needed.
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 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
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