Pfizer

Medical Director

• Plan and execute independent Medical strategy and engagement for appropriate assigned external medical stakeholders 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 external medical stakeholder insights, providing requested information to external medical stakeholders as allowed by Pfizer guidance and sharing external medical stakeholder viewpoints with Pfizer as appropriate
• Understand the priorities of Pfizer Medical Affairs in order to contribute to Medical educational content strategy development and execute aligned Field Medical tactics
• Maintain effective and appropriate communication and collaboration among headquarters Medical colleagues, Medical Information, and other Pfizer Field Medical colleagues
• Demonstrate expertise in scientific 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 care improvements in Medical communications and deliverables, incorporating Health Literacy and cultural awareness principles to ensure that patients remain the ultimate focus
• Conduct all activities in accordance with all relevant policies, procedures and compliance guidance
• Educate external medical stakeholders based on patient care gaps and aligned to medical strategy with the goal of enhancing understanding of disease state and guideline-based care and improve overall patient care
• Achieve leadership-defined expectations regarding the number of external medical stakeholders engaged. Field Medical Role Responsibilities
• Deliver approved medical content about Pfizer medicines and relevant topics in the cardiovascular and metabolic areas.
• Identify and seek medical scientific engagement from priority external medical stakeholder segments in assigned cardiovascular/metabolic area.
• Provide truthful, accurate, and scientifically supported information in response to direct unsolicited medical requests from external medical stakeholders in a manner that complies with all applicable Pfizer guidelines, policies, and procedures
• Leads advisory boards (BRF, Vendor) with manager oversight.
• Field relevant inbound queries from external medical stakeholders via established triage process
• In collaboration with US and/or Global Medical Affairs colleagues, partner with Internal Medicine / Specialty Care 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
• Serve as a Medical resource to HQ Medical Affairs, other Field Medical colleagues, and external Therapeutic Area investigators and researchers as appropriate
• Appropriately provide Medical support throughout the Investigator Sponsored Research (ISR) process
• Cultivate research and therapeutic area 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 external medical stakeholders
• 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

Internal Medicine Field Medical Director, non-MD

• Own end‑to‑end accountability for the EDC platform across strategy, delivery, operations, and value realization
• Define and govern multi‑year product vision and roadmap, aligned with Pfizer clinical and digital strategies
• Facilitate and drive final prioritization and trade‑off decisions across scope, funding, risk, and timeline
• Ensure compliance, data integrity, and audit readiness in partnership with Regulatory, Quality, and IT stakeholders
• Responsible for decisions that impact the overall product vision and metrics (e.g., Objectives & Key Results (OKRs) fulfillment
• Create, maintain, and execute against a prioritized roadmap for the Clinical business
• Establish strong relationships with key business stakeholders and serve as a strategic partner in product decision making
• Work with cross-functional teams of architects, engineers, and designers to deliver customer-centric product features
• Apply user-centered design principles and practices in the product development lifecycle
• Exercise strong decision-making mandate across cross-functional teams
• Stay in sync with the Product Owners on priorities and day-to-day decision making
• Prepare and support the agile team on product demos
• Contribute to the overall success and lifecycle of the product during definition, design, user story/requirement creation, documentation, launch, management updates, and metrics
• Oversee creation of user stories/specs and data analysis to justify product decisions and apply key learnings
• Create and deliver presentations to stakeholders and users
• Responsible for managing and/or retiring other CDMS systems (i.e. RAVE, Inform, DMW, OC)

Director, Clinical Technology, EDC Product Manager

Platform Engineer

• Define and own the Data & BI platform strategy and multi-year roadmap, ensuring platform investments are aligned to the needs of federated AI and analytics teams across Pfizer
• Lead, develop, and grow a team of engineers and platform specialists across Platform Operations, Platform Development, and Data Reliability pods
• Establish and maintain product-minded ownership of the platform portfolio with roadmap priorities driven by user needs
• Own the vendor relationships and licensing strategy for the data and BI platform portfolio, including contract management, performance governance, and technology evaluation
• Partner with the Head of AI Ready Data to ensure platform infrastructure and data governance standards are tightly integrated
• Oversee the design, build, and operation of enterprise data pipelines, warehouse/lakehouse environments, and BI infrastructure at scale
• Define and publish platform SLAs covering availability, data freshness, query performance, and pipeline reliability
• Drive platform cost transparency and FinOps practices ensuring compute and storage costs are visible and continuously optimized
• Ensure all platforms meet Pfizer's enterprise security, privacy, and regulatory compliance requirements
• Serve as the primary platform interface for federated AI and analytics teams across Pfizer, embedding platform support and enabling self-service access
• Report regularly to the Chief AI and Data Officer on platform health, SLA performance, adoption metrics, and investment priorities

Head of Data, BI Platform Engineering

• Own the infrastructure layer for Pfizer's AI ambitions
• Manage the compute, LLM gateway, MLOps machinery, and observability platform
• Architect the AI workloads platform to support various Pfizer domains
• Build a governed, automated deployment pipeline for AI models
• Develop agent orchestration layer and observability infrastructure
• Monitor real-time usage and anomaly detection for AI systems
• Oversee MLOps platform, experiment tracking, model versioning, and deployment pipelines
• Ensure compliance with Trusted AI's governance policies

Head of AI – Agentic Platform Engineering

Research Analyst

• Lead site management and monitoring activities across assigned clinical trial sites, ensuring studies are conducted in accordance with protocol, Good Clinical Practice (GCP), regulatory requirements, and Pfizer standards.
• Serve as the primary point of contact for investigator sites, building strong partnerships to support high-quality study delivery and successful trial outcomes.
• Manage site operations from study start-up through closeout, ensuring key milestones, timelines, and quality objectives are achieved.
• Conduct onsite, remote, and risk-based monitoring activities, including site initiation, routine monitoring visits, and closeout visits.
• Partner with Site Care Partners and cross-functional study teams to identify and mitigate risks, resolve site issues, and drive operational excellence.
• Support patient recruitment and enrollment efforts by collaborating with investigators and study teams to address site-level challenges and implement recruitment strategies.
• Provide protocol guidance, training, and coaching to investigator site personnel to ensure compliance, quality execution, and patient safety.
• Develop and maintain strong scientific and operational knowledge of study protocols, investigational products, and therapeutic areas to effectively support investigators and site teams.
• Drive the identification, escalation, and resolution of site quality, compliance, and data integrity issues, including implementation of corrective and preventive actions (CAPAs).
• Monitor and support patient safety activities, including adverse event and serious adverse event reporting and follow-up.
• Ensure timely completion and maintenance of essential study documentation, trial records, and regulatory compliance requirements throughout the study lifecycle.
• Contribute to continuous improvement initiatives by mentoring junior CRAs, sharing best practices, and participating in local and regional process improvement projects.

Clinical Research Associate – Senior

Manager

• Design and adapt health economic models (e.g., cost-utility, cost-effectiveness, budget impact) to support HTA submissions across countries within the cluster.
• Generate and synthesize clinical and economic evidence, including SLRs, NMAs, and real-world data inputs.
• Prepare value dossiers and submission packages aligned with national and regional HTA requirements.
• Apply AI-enabled tools for literature review automation, scenario modeling, and data visualization.
• Support the end-to-end HTA submission process, ensuring accuracy, consistency, and compliance with internal and external standards.
• Conduct internal review checkpoints and collaborate with cross-functional teams to address uncertainties and strengthen value propositions.
• Maintain documentation and version control for all HTA deliverables across markets.
• Work closely with the HTA Lead, Medical and Commercial teams to align technical outputs with strategic objectives.
• Contribute to internal knowledge sharing by documenting learnings and best practices from HTA projects.
• Participate in cluster-wide HTA hub activities and support harmonization of processes across cluster.
• Prepare materials for payer interactions, advisory boards, and external consultations.
• Contribute technical input to policy shaping initiatives led by the HTA Lead or cluster teams.

Senior Manager, Cluster HTA Hub

• Join a team of scientists supporting oncology development programs
• Act as Clinical Pharmacology Lead providing pharmacology expertise to multidisciplinary project teams
• Provide clinical pharmacology components to Clinical Study Protocols, Reports, and plans
• Plan, design, and oversee clinical pharmacology studies with operational assistance
• Implement model-based drug development using quantitative approaches
• Execute PK analysis and conduct appropriate PK/PD analyses
• Integrate knowledge of pharmacokinetics, pharmacodynamics, and patient characteristics to optimize doses
• Provide recommendations for clinical doses and dosing regimens
• Contribute to all regulatory documents and support resolution of queries from drug regulatory agencies

Manager, Clinical Pharmacology

• Provide cardiovascular-metabolic therapeutic/product expertise for the designated therapeutic area across a broad range of external medical stakeholders
• Plan and execute independent Medical strategy and engagement for appropriate assigned external medical stakeholders within a territory
• Maintain required level of knowledge of relevant TA/disease states and Pfizer medicines
• Serve as a conduit and resource for Medical Information and external medical stakeholder insights
• Optimize patient care improvements in Medical communications and deliverables
• Educate external medical stakeholders based on patient care gaps
• Achieve leadership-defined expectations regarding the number of external medical stakeholders engaged
• Deliver approved medical content about Pfizer medicines and relevant topics in the cardiovascular and metabolic areas

• Plan and execute independent Medical strategy and engagement for assigned external medical stakeholders
• Maintain required level of knowledge of relevant TA/disease states and Pfizer medicines
• Serve as a conduit and resource for Medical Information and external medical stakeholder insights
• Understand the priorities of Pfizer Medical Affairs for content strategy development and Field Medical tactics execution
• Optimize patient care improvements in Medical communications
• Educate external medical stakeholders based on patient care gaps
• Achieve leadership-defined expectations regarding external medical stakeholders engaged
• Deliver approved medical content about Pfizer medicines and relevant topics
• Identify and seek medical scientific engagement from priority external medical stakeholder segments
• Provide truthful, accurate, and scientifically supported information in compliance with applicable Pfizer guidelines and policies

Internal Medicine Field Medical Director, MD

General

• Drive sales in assigned territory to maximize approved business objectives
• Engages with customers both face to face and virtually
• Develops and implements effective business and territory call plans; effectively identifies and implements live/virtual engagement strategies with customer to maximize overall effectiveness and impact
• Effectively builds rapport and relationships with customers in both live and virtual environments; uses judgment to maintain customer engagement by successfully utilizing existing and ever-changing digital tools effectively for successful customer engagement
• Understands and leverages internal reports and analytics to assist with identifying, developing, and implementing strategic business opportunities
• Compliantly leverages product and disease state knowledge using approved clinically oriented disease state information and patient resources, as applicable
• Demonstrates market knowledge, uncovering barriers and drivers across all relevant business channels (Public Health, Private Market, Retail, etc.)
• Collaborate effectively and compliantly with cross-functional colleagues, including Field Medical and Account Management, to address customer inquiries and advance Pfizer objectives
• Completes all administrative expectations on time and compliantly (e.g., entering customer calls appropriately, submitting expenses, responding to all requests from sales leadership, managers and/or Pfizer internal partners)

Vaccines Specialist, Health and Science

Full-stack Engineer

• Lead a team of Software Engineers to design, build, and maintain software systems
• Focus on code quality, architecture decisions, and reliable delivery
• Drive delivery of critical technical initiatives and platforms
• Shape technology-driven business strategy and represent technical perspectives at the executive level
• Establish SLOs/SLIs across teams and mentor engineers on reliability practices
• Document technical standards and processes across the organization
• Transform organizational practices around curiosity and continuous learning
• Enable cross-disciplinary learning and inspire holistic solutions

Senior Director, Engineering Lead

• Ensure proper conduct of clinical trials in accordance with applicable laws, Good Clinical Practices, and Pfizer standards
• Serve as the primary point of contact for assigned investigator sites
• Conduct onsite, remote/electronic monitoring as needed for study site activities
• Monitor site level AEs and SAEs and collaborate with the Drug Safety Unit
• Submit all required reports, documentation, updates within required timeframes
• Identify and resolve investigator site issues within required timeframes
• Ensure quality of site delivery

Senior Clinical Research Associate

AI Engineer

• Set and lead the storytelling strategy for Pfizer’s AI-native engineering transformation, translating platform capabilities and engineering impact into narratives that resonate across the organization and shape how executive leadership understands the value being created.
• Define and lead the strategic approach to high-impact live moments (showcases, demo days, and events) that put builders’ work in front of peers and senior stakeholders
• Deliver a regular cadence of flagship storytelling pieces that raise the visibility and credibility of the team’s work and influence executive leadership’s continued confidence and investment.
• Establish and lead a systematic communications operating model across the organization, including a shared content calendar, reliable content-sourcing pipelines from engineering teams, and clearly defined roles and responsibilities within the team.
• Own the storytelling and communications budget, resourcing a core team supplemented by contract talent to deliver exceptional creative output.
• Directly lead, coach, and develop a high-performing storytelling team, complemented by contract and agency talent. Setting clear goals and priorities, managing performance, and building the team’s bench strength and capabilities over time.
• Own the creative agency relationship lifecycle. From sourcing and selection through briefing, creative direction, and ongoing performance management to ensure external partner consistently deliver exceptional work.
• Apply an audience-first approach to content strategy, tailoring formats, channels, and creative execution to the preferences and needs of each target audience, from individual engineers to the executive leadership team.
• Build and leverage strong relationships across engineering and senior leadership to source stories directly from the work, understanding what is being built, for whom, and why it matters. Use that insight to shape strategic communications priorities.
• Establish and track success measures focused on builder engagement, community growth, and leadership confidence, and use these insights to inform team strategy and continuous improvement.
• Anticipate and manage the organizational change involved in shifting how Pfizer engineers work and are perceived, preparing engineering and business stakeholders across the organization for new ways of working.

Communications & Storytelling Lead, AI-Native Engineering

• Drive customer engagement and sales performance through effective in-person and virtual interactions across endocrinology accounts
• Build strong, compliant relationships with endocrinologists, advanced practice providers, multidisciplinary care teams, and office staff across assigned accounts
• Deliver approved promotional and disease-state messaging to support appropriate Endocrinology product use
• Leverage product, disease, and market knowledge to identify opportunities, prioritize accounts, and support appropriate patient identification and referral pathways in endocrine disease
• Support patient access by providing information on prior authorization requirements, reimbursement support, hubs, and co-pay resources as applicable
• Compliantly collaborate with cross-functional partners to address customer needs, remove access barriers, and advance Endocrinology business objectives
• Use digital tools and insights to plan, execute, and optimize Endocrinology territory activities

Senior Health and Science Specialist, Rare Endocrinology

Representative

• Engage with customers in-person and virtually to grow the business and drive product demand
• Provide solutions to achieve business objectives
• Implement strategies that drive HCP digital engagement adoption
• Develop and execute territory business plan in line with business objectives

Internal Medicine Field Medical Director, non-MD

Director, Clinical Technology, EDC Product Manager

Head of Data, BI Platform Engineering

Head of AI – Agentic Platform Engineering

Clinical Research Associate – Senior

Senior Manager, Cluster HTA Hub

Manager, Clinical Pharmacology

Internal Medicine Field Medical Director, non-MD

Internal Medicine Field Medical Director, MD

Vaccines Specialist, Health and Science

Senior Director, Engineering Lead

Senior Clinical Research Associate

Communications & Storytelling Lead, AI-Native Engineering

Senior Health and Science Specialist, Rare Endocrinology

Health Representative – Primary Care