Pfizer

Director

• Serve as a strategic thought partner and operational lead, or “control tower,” for the OPSA Patient Solutions Innovation team
• Develop, evolve, and lead projects and programs advancing Pfizer Oncology Patient Solutions platforms, including Pfizer Oncology Together, This is Living with Cancer, and My Healthcare Finances
• Develop and implement team priorities, evaluate strategic trade-offs, and identify downstream impacts across OPSA
• Identify and prioritize major projects, processes, and resources to support operating plans and OPSA priorities
• Link OPSA strategy and marketing initiatives to oncology imperatives and measurable organizational outcomes
• Leverage third-party, field reimbursement, patient advocacy insights, and research to assess market and patient trends
• Lead Patient Solutions strategic planning within the broader OPSA and OBU strategic planning process
• Lead Patient Solutions budget management and operating plans across teams
• Identify themes and lead initiatives to educate and train customer-facing and headquarters colleagues
• Design and execute training and communication plans supporting Pfizer Oncology Patient Solutions platforms
• Lead OPSA FBSTs and collaborate on congress strategy and execution
• Track and synthesize KPIs and program performance data for leadership and cross-functional partners
• Translate data and insights into leadership-ready presentations and communications
• Support responsible integration of AI and digital tools into patient-facing programs
• Identify opportunities to use technology, digital tools, and platforms to improve enablement and operating efficiency
• Coordinate cross-functional work across OPSA, Marketing, Sales, Key Account Management, Digital, Medical Affairs, and Commercial Strategy
• Drive coordination with enablement leaders across other business units to identify synergies and share best practices
• Represent Oncology Patient Solutions and contribute to continuous improvement processes

Oncology Patient Solutions Director

Medical Director

• Provide medical and scientific expertise and oversight for clinical trials
• Serve as a single point of accountability for study design, execution, monitoring, delivery, reporting, and patient safety
• Develop strategies for protocols intended to obtain worldwide approval
• Provide medical advice for risk assessment, mitigation planning, and safety issues
• Review individual-subject and cumulative safety data and monitor serious adverse events
• Participate in Safety Review Teams, Data Monitoring Committees, steering committees, and other study bodies
• Review literature and communicate safety information to study sites
• Provide medical input into clinical development plans, protocols, informed consent documents, and country feasibility
• Support study teams with monitoring guidelines, statistical analysis plans, data quality planning, and clinical review activities
• Contribute to CRO/vendor selection and ensure protocol, clinical, data-integrity, and timeline requirements are met
• Conduct medical review and interpretation of efficacy and safety data
• Collaborate on top-line reports and clinical study reports, ensuring scientific validity, quality, and timeliness
• Provide protocol-specific training to study teams, investigators, and clinical research associates
• Monitor investigator compliance with protocols and regulatory requirements
• Support issue resolution, study closeout, audit responses, and inspection readiness
• Author clinical sections of regulatory documents and contribute to abstracts, posters, presentations, and publications
• Interact with regulatory authorities, key opinion leaders, and principal investigators
• Build key opinion leader and principal investigator networks for new trials

Clinical Development Medical Director, MD required

Manager

• Develop and execute high-quality HTA, Value & Evidence strategic efforts to support optimal access and reimbursement for Oncology treatments
• Provide strategic guidance and robust evidence development to support global patient access
• Manage health economics and outcomes research to generate data supporting patient access to the genitourinary cancer portfolio
• Collaborate with Oncology cross-functional teams, country teams, and the Global Access Strategy and Pricing team
• Support development of the Global HTA Value & Evidence Strategy
• Manage clinically relevant and scientifically valid Value & Evidence studies and projects, including non-interventional studies and registries
• Lead updates of global value dossiers, economic models, and innovative value-proposition tools
• Develop real-world evidence generation strategies and execute studies
• Coordinate input from local and regional Access & Value teams on evidence needs
• Lead data dissemination plans and communicate evidence through publications and conference presentations

Senior Manager, HTA, Value and Evidence, Genitourinary Cancer

• Shape the strategic direction of Pfizer's Global Hospital & Biosimilars portfolio
• Develop enterprise recommendations on where the business should grow, defend, improve, simplify, rationalize, or exit
• Lead the Annual Portfolio Review and own portfolio recommendations across GH&B value chains
• Translate strategic theses into decision-ready recommendations with assumptions, risks, trade-offs, dependencies, and enterprise implications
• Present and defend recommendations in the Global Portfolio Forum and other governance forums
• Maintain a current portfolio opportunity pipeline and identify emerging opportunities and risks
• Lead or co-lead high-priority portfolio assessments and determine appropriate scope, analytical approach, evidence, and cross-functional engagement
• Assemble and direct cross-functional teams across Commercial, Manufacturing, Finance, Regulatory, Medical, Quality, Digital, and market organizations
• Guide recommendations from assessment through governance and transition to execution
• Own and continuously improve the GH&B value assessment methodology
• Define decision questions, metrics, analytical views, and visualization capabilities for actionable portfolio insights
• Apply AI-enabled analytics responsibly while ensuring validated data lineage, transparent assumptions, and human judgment
• Shape AI-enabled analytics and visualization capabilities for portfolio performance, value creation, and emerging opportunities
• Establish scalable approaches that accelerate business questions into decision-ready insights and enable self-service access
• Translate portfolio performance signals into actionable optimization opportunities
• Build enterprise partnerships and resolve cross-functional implications, dependencies, and trade-offs
• Evaluate market trends, competitive developments, customer needs, and industry practices for enterprise impact
• Represent and advocate for the enterprise perspective when functional, geographic, or market priorities compete
• Occasional business travel of 10–15%

Director, Portfolio Strategy – Management

• Lead a defined portfolio of state policy priorities and government relations responsibilities in Iowa, Minnesota, and other states identified by SPGR leadership
• Develop and support implementation of coordinated national and state policy positions and strategies aligned with business and enterprise objectives
• Serve as enterprise-wide subject matter expert and point of accountability for assigned state policy issues
• Develop policy platforms, principles, legislative language, backgrounders, research summaries, comment letters, testimony drafts, and talking points
• Analyze, forecast, and communicate legislative and regulatory developments and their implications to internal stakeholders and senior leaders
• Develop strategies to generate policy evidence through consulting firms and academics
• Participate in trade association workgroups and represent Pfizer in policy coalitions, forums, and legislative hearings
• Develop strategies to influence the policy environment and state policymakers, regulators, government officials, opinion leaders, and the public
• Monitor state legislation and regulations affecting Pfizer policy priorities
• Identify and analyze emerging political and policy issues
• Develop and execute lobbying strategies
• Collaborate with Pfizer colleagues, contract lobbyists, and third-party stakeholders to achieve legislative and regulatory objectives
• Supervise outreach and communication to state and local policymakers
• Supervise grassroots and political action programs and maximize PAC and advocacy impact
• Plan and manage a budget within established guidelines

Director, State Policy – Government Relations

General

• Lead ICET's global launch activation portfolio and translate business, brand, medical, and launch-readiness requirements into integrated training content and capability activation plans
• Establish an enterprise view of launch capability demand, portfolio dependencies, capacity constraints, sequencing risks, and reuse opportunities
• Recommend launch activation priorities and trade-offs to ICET, GCET, and launch leadership; escalate decisions requiring broader alignment
• Serve as ICET's strategic launch activation partner to Commercial Excellence, Brand, Medical, Launch Excellence, Regional, Capability Architecture, and GCET Delivery teams
• Govern launch content activation across disease-state, product, competitive, applied-skill, coaching, reinforcement, and performance-support content
• Apply established capability and learning architecture to move customer-facing colleagues from awareness and knowledge to application and confident execution
• Set requirements for modularity, reuse, localization, and AI-enabled content development across markets
• Define launch capability measures including content availability, training readiness, adoption, confidence, application, and reinforcement
• Connect training and capability indicators with launch-readiness and business-outcome measures
• Lead launch-related content governance and cross-functional issue resolution
• Oversee external partners supporting launch content and capability activation
• Transition approved content and activation plans to GCET and market delivery teams with requirements, timing, readiness checkpoints, and feedback loops
• Advise senior leaders on launch capability readiness, portfolio insights, risks, resource implications, and recommended actions
• Continuously improve ICET's launch activation operating model and codify repeatable practices
• Accommodate periodic early morning or evening engagements with international markets
• Travel domestically and internationally approximately 15–25%

Global Launch Activation Lead

Content Marketing Manager

• Lead translation of business and brand priorities into integrated capability experiences across Pfizer’s portfolio
• Partner with the TRIAD, Business Units, Customer Engagement Training, Launch Excellence, and Brand Delivery to build activation plans, learning journeys, and content strategies
• Own portfolio intake, prioritization, activation planning, content orchestration, and experience design
• Serve as primary activation partner on capability priorities, content investment, and activation sequencing
• Translate business and portfolio priorities into a coordinated capability, content, and activation roadmap
• Identify capability gaps, readiness risks, and activation dependencies and recommend mitigation strategies
• Design connected learning journeys incorporating content, practice, coaching, reinforcement, and performance support
• Integrate product knowledge, disease-state education, competitive intelligence, and market/customer insights into cohesive experiences
• Select appropriate instructor-led, digital, coaching, simulation, and microlearning modalities
• Own portfolio-wide intake, prioritization, and routing of capability and content requests
• Govern content lifecycle from creation through retirement and determine build-vs-reuse-vs-adapt approaches
• Design for enterprise reuse and global scalability with regional and market teams
• Maintain visibility into portfolio status, dependencies, capacity, cost, and risk
• Apply AI-enabled solutions to content development, insight curation, personalization, simulation-based learning, and activation efficiency
• Partner with Digital, Analytics, AI, and GCET stakeholders on AI-enabled activation capabilities
• Ensure AI-supported processes align with Medical, Legal, Regulatory, GCMA, and organizational governance requirements
• Equip CET and Brand Delivery teams with content, coaching resources, simulations, and performance-support tools
• Lead cross-functional alignment across internal teams, vendors, subject matter experts, and governance stakeholders
• Influence decisions and drive outcomes in a highly matrixed environment without direct authority
• Define activation success measures aligned to portfolio priorities and business outcomes
• Use readiness, learner, and performance data to assess effectiveness and identify improvements
• Monitor adoption, content utilization, enterprise reuse, efficiency, and scalability trends
• Optimize content strategies, activation approaches, and portfolio-routing decisions based on data and stakeholder input

Global Portfolio Content Activation Lead

Account Manager

• Serve as GCET's enterprise lead for healthcare ecosystem trends, market and customer insights, external partnerships, and Business of Healthcare learning content
• Track shifts in care delivery, payment models, technology, policy, and customer dynamics across U.S. and international markets
• Translate external developments into market content, curricula, insights, recommendations, and enterprise perspectives
• Identify emerging trends, capability gaps, risks, and opportunities relevant to customer-facing readiness
• Apply analytics and intelligence tools consistent with enterprise AI governance standards
• Build and maintain relationships with academic institutions, professional associations, healthcare innovators, and industry experts
• Curate external research and best practices and connect market dynamics to organizational strategy
• Evaluate partnership opportunities against business priorities and future capability needs
• Represent Pfizer at conferences, advisory forums, and industry events
• Develop and maintain role-based Business of Healthcare curricula and market-focused learning content
• Build enterprise-level market intelligence frameworks and learning resources across therapeutic areas and business units
• Translate complex healthcare and customer intelligence into learning content supporting readiness, capability development, and activation planning
• Develop enterprise perspectives on future trends and support long-range planning
• Inform launch strategies through market insights and associated training needs
• Travel regularly domestically and internationally for conferences, academic partnerships, and industry engagements

Director, Enterprise Market Intelligence & Strategic Partnerships

Scientist

• Lead, manage, support, and develop the national BU Medical Affairs Scientist team in the lung therapeutic area
• Jointly develop team objectives with the BU Medical Director
• Develop the Medical Plan and oversee local implementation
• Recruit, manage, coach, and continuously develop team members
• Prioritize team activities, resources, and budgets based on local needs, medical priorities, and performance metrics
• Integrate the team into local, regional, and global Pfizer networks
• Build and maintain peer-to-peer relationships with HCPs, KOLs, patient organizations, professional societies, payers, regulators, HealthTech companies, digital health agencies, and AI regulatory authorities
• Engage in scientific exchange with HCPs and critically evaluate and contextualize scientific and AI-generated evidence
• Generate, document, synthesize, and share medical insights
• Support pipeline development, including protocol feasibility, site identification, and ISR/IIR projects
• Lead local RWE generation, including AI-supported study design and EHR-based feasibility analysis
• Collaborate with Commercial, Access & Value, Regulatory, Legal, and Compliance while maintaining non-promotional boundaries
• Ensure compliance with legal, regulatory, and Pfizer internal requirements, as well as Responsible AI and data governance standards

Lead Medical Affairs Scientist – Lung Field

• Provide medical and scientific expertise and oversight for one or more clinical trials
• Serve as the single point of accountability for study design, execution, monitoring, delivery, reporting, and patient safety
• Develop strategies for protocols intended to obtain worldwide compound approvals
• Oversee study safety, including safety surveillance plans, individual and cumulative safety data review, SAE reporting, and benefit-risk assessments
• Participate in Safety Review Teams, Data Monitoring Committees, steering committees, and other study bodies
• Review literature and communicate safety information to study sites
• Provide medical input into clinical development plans, protocol design, country feasibility, and study strategy
• Ensure protocols, informed consent documents, and related documents meet regulatory and company requirements
• Provide clinical input on monitoring guidelines, statistical analysis plans, clinical review forms, data edit checks, and data quality planning
• Contribute to CRO/vendor selection and ensure medical and technical data-integrity requirements are applied
• Review and interpret clinical trial efficacy and safety data
• Deliver top-line reports and clinical study reports in collaboration with statisticians and medical writers
• Ensure medical and scientific validity of study reports and conclusions
• Disclose appropriate safety and efficacy data through ClinicalTrials.gov, EudraCT, or Pfizer.com
• Provide protocol-specific training to study teams, investigators, clinical research associates, and others
• Interact with healthcare professionals, regulatory authorities, key opinion leaders, and principal investigators
• Monitor investigator compliance with protocol and regulatory requirements
• Support issue resolution, study closeout, audit responses, and inspection readiness
• Author clinical sections of regulatory documents, including Investigator Brochures, Annual Reports, IND sections, and clinical study reports
• May co-author abstracts, posters, presentations, and publications
• May contribute to protocol budget execution
• Liaise with key opinion leaders and principal investigators to build networks for new trials

• Develop and execute high-quality HTA Value & Evidence strategic efforts to support optimal access and reimbursement for Oncology treatments
• Provide strategic guidance and robust evidence development to achieve global patient access by demonstrating the value of Oncology medicines
• Manage health economics and outcomes research to generate data supporting patient access to the genitourinary cancer portfolio
• Work closely with Oncology cross-functional teams, including access, medical, clinical, and commercial teams, and country teams
• Support development of the Global HTA Value & Evidence Strategy
• Manage clinically relevant and scientifically valid Value & Evidence studies and projects, including non-interventional studies and registries
• Lead updates of global value dossiers, economic models, and innovative tools supporting the value proposition
• Develop real-world evidence generation strategies and execute studies
• Coordinate input from local country/regional Access & Value teams on evidence needs
• Lead data dissemination plans and communicate evidence through publications and conference presentations
• Align with the Global Access Strategy and Pricing team and Oncology cross-functional teams on strategy and project execution

Senior Manager, HTA, Value and Evidence – Genitourinary Cancer

• Lead a defined portfolio of state policy priorities and government relations responsibilities in Iowa, Minnesota, and other states identified by SPGR leadership
• Develop and support implementation of coordinated state policy positions and strategies aligned with business and enterprise objectives
• Serve as enterprise-wide subject matter expert and point of accountability for assigned state policy issues
• Develop policy platforms and materials including policy principles, legislative language, backgrounders, talking points, research summaries, comment letters, and testimony
• Analyze, forecast, and communicate implications of state legislative and regulatory developments
• Develop strategies to generate policy evidence through contracted resources, consulting firms, and academics
• Participate in trade association workgroups and represent Pfizer in policy coalitions, forums, and legislative hearings
• Monitor state legislation and regulations affecting Pfizer priorities in assigned geography
• Identify and analyze emerging political and policy issues
• Develop and execute lobbying strategies
• Coordinate with Pfizer colleagues, contract lobbyists, and third-party stakeholders to achieve legislative and regulatory objectives
• Supervise outreach and communication to state and local policymakers
• Supervise grassroots and political action programs
• Maximize advocacy and public affairs efforts with internal and external groups
• Plan and manage a budget within established guidelines
• Collaborate across Business Units, Legal, Public Affairs, Federal Policy, Market Access, and Corporate Affairs

AI Engineer

• Define technical strategy and architecture for Python-based AI backend platforms using FastAPI
• Architect scalable, reliable, and secure AWS systems using Lambda and EKS
• Drive technical decisions affecting organization-wide engineering practices and platform capabilities
• Design and champion AI system observability using LangChain, Langfuse, and litellm
• Establish standards for monitoring, logging, observability, and operational excellence
• Lead initiatives to optimize performance, security, and scalability of large-scale AI applications
• Mentor and technically guide engineers through code reviews, architecture reviews, and technical leadership
• Identify technical debt, performance bottlenecks, and architectural limitations and drive long-term solutions
• Collaborate with engineering leadership, product, and stakeholders to align technical strategy with business objectives
• Influence technology choices, design patterns, and best practices across the AI Software & Operations department
• Represent the team in organization-wide technical discussions and drive adoption of innovative solutions

Staff Software Engineer – AI Backend Services

Account Specialist

• Drive customer engagement and sales performance through effective in-person interactions across Hemophilia Treatment Centers, healthcare providers, multidisciplinary HTC care teams, and community hospitals
• Build compliant relationships with hematologists, HTCs, and multidisciplinary care teams across assigned accounts
• Deliver approved promotional and disease-state messaging to support appropriate Hemophilia product use
• Use product, disease, and market knowledge to identify opportunities, prioritize accounts, and support appropriate treatment options
• Support patient access by providing information on prior authorization requirements, reimbursement support, hubs, and co-pay resources
• Collaborate with cross-functional partners to address customer needs, remove access barriers, and advance Hemophilia business objectives
• Use digital tools and insights to plan, execute, and optimize Hemophilia territory activities
• Reside within a workable distance of all points of business within the assigned territory
• Travel to all accounts and office locations within the territory; stay overnight as necessary based on territory size and business need

Rare Disease Account Specialist – Hemophilia

• Drive customer engagement and sales performance through effective in-person interactions across Hemophilia Treatment Centers, healthcare providers, multidisciplinary HTC care teams, and community hospitals
• Build compliant relationships with hematologists, HTCs, and multidisciplinary care teams across assigned accounts
• Deliver approved promotional and disease-state messaging to support appropriate Hemophilia product use
• Leverage product, disease, and market knowledge to identify opportunities, prioritize accounts, and support appropriate treatment options
• Support patient access by providing information on prior authorization requirements, reimbursement support, hubs, and co-pay resources
• Collaborate with cross-functional partners to address customer needs, remove access barriers, and advance Hemophilia business objectives
• Use digital tools and insights to plan, execute, and optimize Hemophilia territory activities
• Reside within a workable distance of all points of business within the assigned territory
• Travel to accounts and office locations within the territory, including overnight stays as necessary

Oncology Patient Solutions Director

Clinical Development Medical Director, MD required

Senior Manager, HTA, Value and Evidence, Genitourinary Cancer

Director, Portfolio Strategy – Management

Director, State Policy – Government Relations

Global Launch Activation Lead

Global Portfolio Content Activation Lead

Director, Enterprise Market Intelligence & Strategic Partnerships

Lead Medical Affairs Scientist – Lung Field

Clinical Development Medical Director, MD required

Senior Manager, HTA, Value and Evidence – Genitourinary Cancer

Director, State Policy – Government Relations

Staff Software Engineer – AI Backend Services

Rare Disease Account Specialist – Hemophilia

Rare Disease Hemophilia Account Specialist