Pfizer

Medical Director

• The Global Medical Director will serve as an expert in the IBD field.
• Lead with integrity and be a role model for medical professionalism and scientific excellence.
• Partner cross-functionally with medical teams, health and value functions, clinical development, legal, compliance, and commercial teams.
• Support launch activities and collaborate with country medical teams.
• Demonstrate deep data and disease area expertise for Velsipity and gastroenterology.

Global Medical Director, Gastroenterology

Director

• Develops, coaches, and leads the Cardiac Rare Regional Sales Team to deliver customer value and achieve agreed-upon sales objectives
• Partners closely with other RBDs, the Rare Disease Sales Leadership Team, and other HQ functions
• Builds, coaches, and develops a high-performing leadership bench through hiring, onboarding, training, and performance management
• Creates and sustains an inclusive Patients First culture that drives engagement, retention, and performance
• Monitors performance and market dynamics; translates analytics into coaching, prioritization, and course-correction actions
• Optimizes resource deployment to improve execution quality and profitability
• Role-models a culture of compliance; partners with Compliance and Legal to support routine monitoring

Regional Business Director – Rare Cardiac

Manager

• Lead market research efforts for PADCEV by providing unbiased, objective, in-depth insights to inform business strategies and decisions.
• Identify business questions, design and conduct appropriate and relevant research plans.
• Embed an external market and customer point-of-view to drive strategic direction of brand business and lifecycle management.
• Proactively identify and diagnose business questions, initiate and conduct research, and deliver insights and actionable recommendations across the lifecycle of the product(s).
• Effectively present insights to various stakeholders.
• Collaborate with other Oncology Commercial Analytics partners to help synthesize all available information to produce a comprehensive point of view and deliver clear and actionable recommendations.
• Monitor brand performance and conduct ongoing brand performance tracking.
• Execute brand research plan to drive business impact and deliver insight-based recommendations aligned with brand’s goals and strategy.
• Identify informational gaps within the Market Research Insights team and plan and coordinate efforts to address those gaps.

Senior Manager, Market Research Insights

• Plan and execute medical strategy and engagement for appropriate assigned customers within a territory, compliantly coordinating with other Pfizer colleagues as needed to achieve medical objectives
• Maintain required level of knowledge of relevant TA/disease states and Pfizer medicines, providing therapeutic area/product information to both internal and external stakeholders as needed
• Serve as a conduit and resource for medical information and customer insights, providing requested information to HCPs as allowed by Pfizer guidance and sharing customer viewpoints with Pfizer as appropriate
• Understand the priorities of Pfizer Medical Affairs to contribute to medical content strategy development and execute aligned Field Medical tactics
• Maintain effective and appropriate communication and collaboration among headquarters medical colleagues and other Pfizer Field Medical colleagues
• Demonstrate expertise in communication across multiple channels, including, but not limited to, live and virtual presentations in small or large settings, written communication, and telephone or virtual conversations
• Optimize patient centricity of medical communications and deliverables, incorporating health literacy and cultural awareness principles to ensure that patients remain the ultimate focus
• Deliver approved medical content about Pfizer medicines and relevant topics in the designated therapeutic area
• Identify and seek medical engagement from priority customer segments in assigned TA
• Provide truthful, accurate, and scientifically supported information in response to direct unsolicited medical requests from HCPs in a manner that complies with all applicable Pfizer guidelines, policies, and procedures
• Field relevant inbound queries from HCPs via established triage process
• In collaboration with Global Medical Affairs colleagues, partner with Oncology Research & Development and Global Product Development (GPD) in the identification of potential sites for Pfizer-sponsored clinical trials, including identification of sites serving under-represented patient populations in trials
• Appropriately provide medical support throughout the Investigator Sponsored Research (ISR) process
• Cultivate research and TA expertise, including familiarity with latest congress data and disease state literature
• Provides asset leadership
• Understand the principles of study design, methodology, data analysis, and interpretation and communicate these concepts with customers
• Strong territory leadership
• Reactively and proactively communicate with local Patient Advocacy Group(s), as appropriate, in close collaboration with Corporate Affairs and HQ Medical Affairs
• Deliver insights on local patient organization structure, capabilities, and patient population needs
• Serve on Medical and/or TA and asset cross-functional committees, as appropriate
• Represent Pfizer Medical Affairs leadership with clinical/professional associations and/or societies, consistently demonstrating medical professionalism in all interactions
• Mentorship – Onboarding partner, ad board and study lead mentor
• Participate in special projects as needed

Oncology Field Medical Director – Non-MD

• Responsible for driving GCP Quality by maintaining ‘quality’ line-of sight for assigned clinical trial programs/protocols
• Ensure program and study level quality oversight
• Drive quality risk management and inspection readiness activities
• Provide Study Team Inspection Readiness guidance and support
• Develop and maintain inspection readiness tools and processes
• Provide strategic input to risk-based quality approaches
• Communicate key quality information across study teams

Asset Quality Lead – Director

AI Engineer

• Develop and Implement AI Solutions: Build and deploy AI/ML models and solutions that support process-heavy workflows (e.g. protocol feasibility and site selection, study start-up etc.) including documentation, and operational reporting.
• Contribute to the automation of manual and repetitive activities to improve speed, quality, and consistency.
• Strengthen Operational Decision-Making: Develop predictive, optimization, and scenario-based models to support clinical trial supply forecasting and operational planning.
• Create and maintain dashboards and decision-support tools that translate complex data into actionable insights for CD&O leadership and operational teams.
• Engineer Production-Grade AI Systems: Implement AI solutions that are aligned with data integrity standards and governance best practices, including model validation, versioning, and monitoring.
• Design and implement AI agentic solutions that can plan and execute multi-step workflows.
• Build robust, production-ready ML and analytics pipelines with a focus on reproducibility and scalability.
• Deploy AI solutions in cloud environments, ensuring reliability, security, and seamless integration with existing systems.
• Collaborate Across Disciplines: Partner closely with CD&O line teams, scientists, and Digital partners to ensure that AI efforts remain tightly aligned to real scientific needs and can be deployed in ways that are trusted, scalable, and adopted in day-to-day work.
• Champion best practices in AI engineering system lifecycle.

Director, AI Engineering – Clinical Development and Operations

Supply Chain

• Lead and manage matrix teams responsible for the end-to-end oversight of supply chain activities required for the provision of investigational product.
• Provide consultation on all aspects of investigational product strategies.
• Identify and manage supply chain risk, managing clinical supply budgets.
• Oversee the end-to-end activities and identify potential risks and develop supply strategies.
• Act as a key Global Clinical Supply point of contact for clinical study teams.
• Provide broad consultation on all aspects of clinical drug supply.

Supply Chain Lead, Secondment 12-18 Months

• Lead day-to-day technical delivery of applied AI projects, participating in architecture, code reviews, and prototyping
• Mentor and develop individual contributors, set team standards, and recruit talent to accelerate delivery
• Maintain hands-on involvement in modeling, data pipelines, and integration work to preserve technical credibility
• Run 2 to 6 week prototype cycles: define scope, design experiments, deliver evaluation metrics, and recommend clear go/no-go decisions
• Translate ambiguous commercial problems into testable hypotheses and rapid experiments that produce actionable results
• Remain deeply hands-on in AI/ML engineering and prototyping
• Ensure prototypes follow robust engineering practices: version control, CI/CD for models, containerization, reproducibility, automated tests, and clear documentation
• Apply MLOps principles for deployment-ready artifacts, including model monitoring and rollback strategies appropriate for regulated environments
• Promote modular, reusable code and extraction of common patterns to reduce rework
• Prepare validated prototypes for structured handoff to industrialization, production, or IT teams with runnable artifacts, runbooks, and acceptance criteria
• Collaborate closely with partner Analytics, Data Science, and IT teams to ensure prototypes align with enterprise architecture and standards
• Support scaled rollouts by providing implementation support during transition from build to operations
• Communicate prototype results, limitations, and recommended next steps to the Senior Director, product owners, and business stakeholders in clear, outcome-oriented terms
• Deliver concise executive summaries and data-backed recommendations to inform prioritization and funding decisions

Director, Applied Intelligence

• Responsible for supervising operations of the District to include hiring, live coaching, virtual coaching, representative development, performance management, and the assignment of key "priority" accounts within the medical community, managing 6-10 representatives.
• Develops and implements strategic plans for the District , business plan, and overall responsibility for budgets at District level in alignment with RBD expectations.
• Ensures effective utilization of promotional material, making valuable contribution to the formulation of marketing plans for the year, measuring efficient implementation of the plans in the field and undertaking regular assessment of marketing activities as an integral part of the total marketing operations
• Proactive data analysis to identify market trends
• Builds relationships with customers and key stakeholders and utilizes content appropriately for engagement
• Coaches representatives on seamlessly connecting cross-functional colleagues reactively to address customer needs and how to use digital tools

Dermatology Area Business Manager

• Responsible for supporting clinical trial(s) and lead subteams in clinical development
• Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring
• Lead peer-to-peer interactions with investigator
• Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities
• Lead and contribute to development and maintenance of clinical trial and regulatory documents
• Oversees and provides clinical development leadership across several study teams
• Collaborates with the Global Development Team to create and refine development strategies
• Represents the company in external engagements or in committee members

Senior Medical Director, Clinical Development – Breast Oncology

• Develop and execute a medical education strategy supporting RSV Adult vaccination in the US
• Partner with cross-functional teams to ensure alignment of medical education and engagement plan across various channels with medical priorities
• Provide vaccine medical expertise and support on behalf of the US Medical Affairs team to cross-functional partners, ensuring alignment of internal communications and training around new and key scientific data on RSV
• Partner cross-functionally within medical to ensure aligned KOLs activities to gather feedback and input into strategy development and execution
• Provide medical review for medical education grants
• Demonstrate expertise in communication across multiple channels, including, but not limited to, live and virtual presentations in small or large settings, and written communication

Medical Director, RSV Adult Vaccine, non-MD

• Support the US Medical Affairs Lead for RSV adult vaccines
• Develop and execute a medical education strategy supporting RSV Adult vaccination in the US
• Partner with cross-functional teams to ensure alignment of medical education and engagement plan
• Provide vaccine medical expertise and support to cross-functional partners
• Ensure aligned KOLs activities to gather feedback and input into strategy development
• Demonstrate expertise in communication across multiple channels

Medical Director, RSV Adult Vaccine

Vice President

• Lead a team and develop portfolio and asset Medical Strategies in collaboration with local Medical Leads
• Partner cross-functionally with various medical teams and commercial teams
• Provide exceptional oversight of environmental, disease state, competitor, asset analysis
• Develop rapid data analytic capacities
• Engage with medical directors of independent networks to develop beneficial solutions enhancing patient care
• Chairs or leads the Global Medical Affairs Team
• Represent medical affairs globally at relevant asset team and committees
• Proactively incorporate patients' & physicians' voices in development strategy
• Ensure country aligned medical input into global commercial strategy

Vice President, Global Obesity Medical Lead

• Serve as the technical anchor of the team by actively contributing to architecture, code, and experimental design
• Remain deeply hands-on in AI/ML and software engineering
• Attract, develop, and retain a focused team of exceptional applied AI engineers and data scientists
• Own a 2 to 6 week rapid prototype cycle framework
• Design and run structured experimentation that converts ambiguous business questions into testable hypotheses
• Enforce strict engineering hygiene in every prototype
• Champion containerization and MLOps frameworks
• Extract reusable patterns, templates, and best practices from successful prototypes
• Lead the responsible and effective adoption of Generative AI tools
• Partner closely with broader Data Science teams to execute structured, well-documented handoffs

Senior Director, Applied Intelligence

• Plan and execute Medical strategy and engagement for appropriate assigned customers
• Maintain required knowledge of relevant TA/disease states and Pfizer medicines
• Serve as a conduit and resource for Medical Information and customer insights
• Understand the priorities of Pfizer Medical Affairs for content strategy development
• Maintain effective communication and collaboration among Medical colleagues
• Deliver approved medical content about Pfizer medicines and relevant topics
• Identify and seek medical engagement from priority customer segments
• Provide truthful, accurate, and scientifically supported information in response to medical requests
• Collaborate with Global Medical Affairs colleagues for clinical trials
• Cultivate research and therapeutic area expertise
• Reactively and proactively communicate with local Patient Advocacy Group(s)