Pfizer

Clinical Research

• Support complex studies or lead low‑complexity studies across the full study lifecycle, including protocol development, training, vendor management, study oversight, data review, and reporting.
• Ensure consistency, quality, patient safety, and regulatory compliance across all assigned studies.
• Collaborate with Medical Evidence Generation (MEG), Medical Affairs, Statistics, Clinical Data Sciences, and external partners.
• Provide operational input into tactical study implementation aligned with asset strategies.
• Identify and resolve operational or scientific issues; escalate as appropriate.
• Represent the Clinical Scientist function in program teams and governance forums as needed.
• Support regulatory submissions, inspections, and audits.
• Present and discuss study data internally and externally (e.g., with KOLs or regulators).
• Contribute to R&D initiatives and process improvement efforts.

Clinical Scientist – m/f/d

Product Designer

• Lead the design efforts within our Forward Impact Teams (FIT Pods)
• Utilize cutting-edge AI tools, rapid prototyping, and lean-team approach
• Collaborate with developers, strategists, and stakeholders to iterate on digital products
• Create, maintain, and evolve design standards, ensuring accessibility compliance
• Deliver end-to-end design for high-impact projects under tight deadlines
• Design and document assistant behaviors and conversational UX

Senior Manager, Experience Design – Agentic & Conversational Product Design

Vice President

• Serve as the primary liaison with business development to define and implement the global oncology business development strategy, oversee due diligence activities, and cultivate high-impact external partnerships.
• Engage with executive leadership and disease area strategy teams to assess portfolio needs, deliver strategic recommendations, and ensure clear, compelling communication of product strategies and updates.
• Advise on the prioritization of both internal and external preclinical and clinical research initiatives, ensuring alignment with organizational goals.
• Provide matrix leadership to early-stage Global Development Product Leaders (GDPLs), clinical scientists, clinical pharmacologists, and other team members within the function.
• Collaborate regularly with leaders and representatives across Pfizer Oncology and partner lines to enhance awareness of emerging targets, priorities, and project status, fostering alignment and influence.
• Lead and participate in Key Opinion Leader (KOL) advisory boards to gather expert feedback on development assets and inform portfolio strategy.
• Conduct comprehensive literature reviews and synthesize findings to support the advancement of clinical development programs in the context of competitive intelligence.
• Champion and deliver on the integration of innovative approaches in early clinical development, including artificial intelligence, translational technologies, model-informed drug development, precision medicine, and other process improvement related initiatives, in order to accelerate decision-making.
• Contribute to organizational excellence within the OESD department by fostering a collaborative, transparent, and trust-based team environment that encourages open communication and alignment with the overall portfolio vision.

Head of External Innovation – Oncology Early Development

Financial Planning and Analysis

• Work directly with regional finance leads and commercial colleagues to understand the monthly performance drivers.
• Prepare revenue and P&L commentary and analysis for review and presentation to Commercial leadership.
• Drive and lead the consolidation and presentation/review of forward-looking components of the FP&A process.
• Lead financial analysis and collaborate with cross functional teams.
• Act as a single point of contact for regional Finance Leads and regional commercial Leadership.
• Lead simplification/automation initiatives and driving other financial process improvements.
• Active participation and support of Global Biopharma FP&A activities as needed.

Senior Manager – Commercial FP&A, Emerging Markets

Program Manager

• Provides comprehensive program management and execution of regulatory strategic and operational deliverables
• Responsible for ensuring all cross-functional regulatory deliverables are achieved on or ahead of schedule and with quality
• Develop regulatory goals in partnership with the Global Regulatory Lead
• Monitors activities across all regulatory team members for operational efficiency ensuring the program delivers on time and within scope
• Directs the regulatory team in the preparation, implementation, maintenance, communication, and management of integrated risk management plans
• Ensures effective, accurate, and timely communication of regulatory information to meet the needs of the product team and stakeholders

Senior Manager, Regulatory Program Management – Submission Strategy, Oncology

Director

• Deliver Region net revenue performance and expense management
• Translate the Business Units vision and strategies
• Drive brand performance and gain market insights
• Lead strategic regional collaboration with marketing & cross functional partners
• Coach team members, document growth goals, and manage performance
• Provide strategic support for enterprise-wide initiatives

Regional Business Director – Hematology

• Provide strategic leadership to shape the team’s overarching vision, guide integrated go‑to‑market strategy development, and drive coordinated tactical execution across the Health Systems, Long‑Term Care, and Urgent Care channels.
• Apply customer insights and market dynamics to guide channel planning and optimize Primary Care portfolio performance.
• Represent the HULC channel perspective in key planning forums to ensure customer and channel considerations inform portfolio strategies.
• Serve as a strategic thought partner to senior leadership, providing channel expertise and customer-informed recommendations.
• Coordinate with leads across marketing, sales, medical, access, and analytics teams to ensure alignment and cohesive execution across the Primary Care franchise.
• Help identify opportunities for innovative, integrated solutions that meet the evolving needs of Health Systems, LTC organizations, and Urgent Care networks.
• Lead, coach, and develop a team of six high-performing colleagues, fostering a culture of accountability, collaboration, and continuous improvement.
• Establish clear priorities, performance expectations, and development plans to build strong channel expertise within the team.
• Oversee the design and execution of operational processes that enable proactive planning and cross-functional coordination across the Primary Care business.
• Drive strong business management discipline to ensure execution excellence and alignment with the broader Customer & Channel Group vision.

Senior Director – Health System, UC, LTC Channels Lead

• Provide comprehensive regulatory program management support
• Ensure alignment with and execution of Pfizer Oncology’s regulatory strategies
• Coordinate and prioritize regulatory activities
• Facilitate decision-making processes
• Oversee information flow to ensure adherence to regulatory timelines
• Partner with regulatory strategists to advance regulatory and submission activities

Manager, Regulatory Program Management – Submission Strategy (Oncology)

Manager

• Ownership and responsibility for post-Rx customer journey design for HCPs, patients, and office staff
• Lead development of all field force training, resources, and assets to support payer pull-through efforts upon launch
• Serve as primary Access point of contact for field force and Key Account Managers; and lead field access advisory team
• Responsible for working with USMA on core materials for Velsipity, incorporating insights from Account Management, Field Sales, GAV, Customer Marketing, Market Access Strategy & Analytics, and other internal and external stakeholders
• Partnering with USMA on the US pull-through strategy, laddering up to LRF access uptake assumptions
• Lead stakeholder alignment, shape brand/account goals, and drive execution with Account Management, Customer Marketing, Contract Strategy, and Sales
• Manage vendor partners in resource development, MLR review and approval
• Lead payer budget management activities including day-to-day tracking, Operating Plan cross-functional alignment and Tactical Plan development

Senior Manager, Payer and Access Integration

Analyst

• Ensure accurate and on-time payment of rebates to assigned accounts.
• Complete analysis on SI rebates to explain variances.
• Ensure adherence to SOX controls and internal SOPs; maintain adequate supporting documentation for rebate payments.
• Collaborate with contracting teams; review draft language for clarity and accuracy as it relates to rebates.
• Provide input into contract negotiation strategies as it relates to payment terms and system capabilities.
• Analyze quarterly finance accruals to verify accuracy and completeness across all assigned accounts.
• Provide ad-hoc account information to WPO Finance for any material changes.

Senior Analyst, Rebates

Marketing

• Develop and execute comprehensive portfolio strategies that impact multiple brands within the oncology umbrella.
• Collaborate with cross-functional teams, including marketing, sales, organized accounts teams, and data analytics.
• Monitor and analyze market trends, competitive landscape, and emerging technologies.
• Prepare and present strategic plans, business cases, and performance reports to senior leadership.
• Partner with BU leaders to develop business strategies.
• Identify key strategic imperatives and capabilities required to achieve these imperatives.
• Lead a portfolio of projects that provide insight and direction for key strategic levers.

Director, Portfolio Marketing

• Lead a team of high functioning individual contributors responsible for driving commercial brand strategy.
• Act as a thought partner to senior US & Global franchise leads on portfolio decisions and overarching strategy.
• Develop and execute creation of in-house knowledge base to drive patient and HCP insights.
• Lead team that develops and monitors key performance metrics to evaluate effectiveness of brand’s marketing campaign.
• Oversee development of Long-Range Forecasts (LRFs) and Operating Plans; ensure accurate effective performance measurement and deliver regular assessments of portfolio performance to leadership.
• Lead dialogue to integrate insights across various GCA cross-functional teams – Data Science, Performance Analytics, etc.

Senior Director, IIS Pediatric Vaccines

• Drive GCP Quality by maintaining quality oversight for assigned clinical trial programs/protocols
• Oversee study-level quality risk management activities including Study Risk Profile development
• Provide Study Team Inspection Readiness guidance and support
• Develop inspection readiness tools and processes
• Communicate key quality information across study teams
• Collaborate with cross functional study team and drive quality risk management activities
• Lead asset level/study level quality risk planning activities

Asset Quality Lead – Oncology

• Lead Pfizer Cardiac Rare Disease Sales efforts within the assigned area in the United States
• Shape and execute the sales strategies for Vyndamax per approved indications
• Supervise and lead Rare Disease Rare Cardiac Senior Health & Science Specialists
• Conduct regular in-field observation and coaching of field representatives
• Ensure effective and compliant promotional communications are delivered to customers
• Maintain required technical expertise to respond accurately to questions regarding products and policies
• Develop Area business objectives and define key performance metrics that are aligned to National Sales and Brand objectives
• Partner with marketing leads & teams to shape brand/customer strategies and initiatives to drive demand

Area Business Manager, Rare Cardiac Disease

• Provides comprehensive program management, ensuring alignment and execution of Pfizer Oncology’s regulatory strategic and operational deliverables
• Responsible for ensuring all cross-functional regulatory deliverables are achieved on or ahead of schedule and with quality that meets or exceeds business needs
• Working with Global Regulatory Lead, responsible for the development of integrated regulatory plan and ensures alignment with the overall strategic and operational plan for the asset
• Offers leadership in regulatory strategy and planning, including development and assessment of scenarios and options, robust decision criteria, risk management, and internal/external communication and stakeholder management strategies
• Develop regulatory goals in partnership with the Global Regulatory Lead and closely monitors progress against these goals for operational efficiency ensuring the program delivers on time and within scope
• Ensures effective, accurate, and timely communication of regulatory information to meet the needs of the product team and stakeholders
• Provides comprehensive project management for regulatory submission activities for initial and supplemental market authorizations