Pfizer

Marketing

• Spearhead global HCP promotional strategy
• Lead messaging strategy and rollout
• Advance RWE strategy for HCP promotion
• Support global launch HCP initiatives
• Ensure robust KPIs are developed and tracked
• Establish strong working relationships with US and ICO teams
• Work closely with global creative agency for message development
• Support management of agency performance and budget

Global HCP Marketing Lead – Secondment 6-8 Months

Product Marketing

• Responsible for executing Go-to-Market excellence (GTM) initiatives
• Ensure GTM activities are performed efficiently
• Coordinate and drive key aspects of the Return-to-Market and launch process
• Support the execution of the US GTM Commercial strategies
• Work cross-functionally to drive accountability, communication, and status reporting across the sterile injectables portfolio

Senior Manager, US Commercial GTM Launch – Secondment, 12 Months

Operations

• Lead country and regional medical operations across MERA
• Provide operational support to the CMAO and partner with the MERA Medical Affairs Leadership Team
• Support effective governance processes/meetings
• Responsible for end to end fit for purpose governance planning/execution
• Lead efforts in partnership with MERA Cluster Medical Lead for Regional Plan development
• Drive change & transformations, working collaboratively with MERA Medical Affairs colleagues
• Lead development of Operating Plan communication for MERA Medical Affairs LT
• Ensure communication between platforms and EM CMAO Operational and Change Excellence
• Driving alignment across MERA on both in-person and omnichannel engagement

Regional Medical Operations Senior Manager

Software Engineer

• Lead the development of AI and data-driven digital products through rapid prototyping and MVP-first approaches
• Define and communicate a clear product vision and strategy
• Collaborate closely with cross-functional teams
• Establish and manage a lean product roadmap
• Drive agile ceremonies and sprint planning
• Champion a culture of experimentation
• Ensure MVPs are scalable and extensible
• Oversee the creation of user stories, prototypes, and wireframes
• Manage stakeholder expectations
• Foster a team environment that embraces ambiguity

Director, Product Manager, Commercial Forward Impact Engineering – Engagement Team

AI Engineer

• Define and communicate the AI transformation vision for Medical Affairs, aligned with enterprise AI strategy and function-specific needs
• Identify high-impact AI use cases across HQ Medical (e.g., Medical Strategy, Publications, Medical Information, Competitive Intelligence) and Field Medical (e.g., Field Medical operations, congress management, advisory boards, ISS/IIRs)
• Prioritize initiatives based on value, feasibility, and strategic alignment, distinguishing commoditized use cases from high-leverage opportunities unique to the organization
• Stay current on emerging AI capabilities (e.g., context engineering, agentic workflows, integration standards such as MCP) and translate them into actionable opportunities
• Build functional prototypes and proofs-of-concept (POCs) that allow stakeholders to experience value before full-scale investment
• Develop and maintain Medical Affairs specific Agent Skills: reusable instruction sets, templates, and domain knowledge packages deployable across multiple workflows
• Create and curate Agent Skills libraries, workflow templates, and context architectures optimized for Medical Affairs applications
• Serve as the primary liaison between Medical Affairs and IT for AI initiatives, translating business needs into technical requirements and vice versa

Medical Affairs Lead

Director

• Partner with Franchise, Value Strategy Leads, USMA, Finance, Analytics, National Accounts and cKAD teams
• Develop and implement innovative provider pricing and contracting strategies
• Lead modeling to support brand financial management and senior leadership endorsement of pricing and contracting strategies
• Develop mid- to long-term ASP forecasts
• Support decision-making for various payer/provider contracting scenarios
• Evaluate ROIs of contracts
• Lead performance tracking leveraging both IQVIA and chargeback data

Director, Biologics Value Strategy

Vice President

• Develop durable business, deepening collaboration with Retail Pharmacy Field Leaders.
• Grow appropriate use of Pfizer Primary Care Retail Pharmacy products.
• Identify shared objectives, align resources, and deploy innovative solutions.
• Engage local stakeholders and manage relationships with field leaders.
• Collaborate closely with various teams to achieve national goals.

Vaccines, VPH AS

Product Manager

• Integrate a single governed International CFC reporting technology roadmap
• Develop coordinated transition plan for CFC Reporting capabilities
• Lead multi year messaging strategy for CFC messaging
• Collaborate with Global Commercial Analytics and marketing teams
• Deliver operational excellence across U.S. and International portfolios

CFC Reporting, Mobile Product Lead

• Drive innovation by working with Commercial business stakeholders and engineers to translate prioritized business opportunities into rapid prototypes and MVPs
• Establish clear product vision, strategy, and roadmaps
• Collaborate closely with commercial stakeholders to align priorities, gather feedback, and adapt solutions
• Lead the development of AI and data-driven digital products through rapid prototyping and MVP-first approaches
• Manage stakeholder expectations by clearly communicating trade-offs, timelines, and outcomes of MVP launches
• Oversee the creation of user stories, prototypes, and wireframes that reflect user-centric design principles

Director, Product Manager – Commercial Forward Impact Engineering & Engagement Team

• Ensure launch readiness across all stakeholder functions
• Provide strategic thought leadership to ensure delivery of a best-in-class launch
• Establish strong partnerships with regional (US, ICO, and EMCO), cross functional, and cross-indication colleagues
• Develop and maintain strong, trusted relationships with all cross-functional partners, incl. medical, access & value, manufacturing/supply, legal, finance, regulatory, clinical, and IIS to have broad oversight into all elements of launch
• Partner with IIS to provide global long-range forecasting guidance to all priority launch markets
• Partner closely with Global Commercial Lead on leadership presentation development and delivery, investor relations and earnings support, and additional leadership deliverables, as needed
• Serve as commercial lead for global launch sequencing and supply launch readiness and prioritization
• Serve as the brand lead for all commercial Enterprise Launch Stage Gates supporting the Launch Excellence organization, including launch tracking platforms and leadership reporting
• Serve as global brand operating plan captain
• Contribute to life cycle management analyses for internal and external opportunities
• Launch performance/KPI tracking: closely monitor early launch market performance, tracking strategic and outcomes KPIs for future market launch optimization and real-time agile launch adjustment, as needed
• Drive a high-performance culture by fostering innovation, customer focus, personal accountability and a commitment for results

Director, Global Vitiligo Launch Lead

Manager

• Development, management, and ongoing maintenance of all data, reporting, analytic tools, platforms and databases for all Commercial Portfolio Management activities
• Leading related initiatives within the Global Marketing Team
• Managing the day-to-day project management and operational effectiveness needs of the Portfolio Planning and Optimization (PPO) lead
• Working across a broad, cross-functional organization
• Develop and manage PPO MS Teams, SharePoint, and other collaboration tools
• Facilitate PPO team cross-projects integration to maintain sustainable data systems and update processes
• Drive, implement and maintain continuous improvement by identifying, developing, and maintaining new capabilities
• Provide thought partnership in building and standardizing commercial reporting eco-system
• Identify and drive technology efficiencies across CPM technical tools
• Project manage activities with CPM, BAI, Digital, Manufacturing, Finance, Business Analytics, Business Technology, Global Marketing, and other departments
• Support the annual revenue and unit alignment process for the LRVF (Long Range Volume Forecast) for the PBG portfolio in partnership with Pfizer Global Supply (PGS), Commercial and Finance

Senior Manager, Commercial Portfolio Planning – Optimization

Risk

• This new secondment role (9-12 months) has accountability for supporting the delivery of IMEX Ecosystem Care for the Process & Solutions Governance council (aka the “CoE” (Center of Excellence)) and the creation of the Standard Work structure for the “CoE.
• Central point of contact / project lead for outlining and implementing IMEx Ecosystem Care for the CoE, providing a timeline / workplan for implementing IMEx Ecosystem Care by end of 2026.
• Collaborate with Change Mgt Lead to determine Change Mgt SW for Ecosystem Care, including but not limited to communication triggers & mechanisms, user adoption, stakeholder mgt, etc.
• Partner with the Director, Performance Intelligence, to outline the structure for Planning and Scheduling “Total System Care”.
• Determine timeline for the implementation of “Total System Care” (TSC) for planning and scheduling workstreams with identification / engagement of key stakeholders for each element of TSC.
• Collaborate with the Planning Business Owner to confirm Planning Ecosystem SW, including but not limited to adherence metrics, CI / backlog tracking & reporting, system health, integration health, etc.
• Collaborate with the Scheduling Business Owner to confirm Scheduling Ecosystem SW, including but not limited to adherence metrics, CI / backlog tracking & reporting, system health, integration health, etc.
• Determine an Ecosystem Health dashboard for visualizing ecosystem health and highlights of exceptions / sources of loss & opportunity.
• Work with nGPS Program Lead / CoE Lead to outline and determine CoE Standard Work, including but not limited to: Standard Work definition, Meeting definition, Meeting cadence, Standard Work templates, including meeting agendas, etc.
• CoE reporting templates and any additional associated Standard Work collateral & processes and visual management tools / dashboards.

IMEx Implementation Lead, Solutions & Process Governance Council – Secondment 9-12 Months

• Ensures scientific integrity and participant safety in clinical trials
• Designs and executes high-quality studies
• Maintains compliance, manages risks and emerging clinical issues
• Supports interpretation and communication of clinical data
• Leads clinical execution of one or more studies of medium - high complexity
• Provides clinical input to development of protocol design document (PDD)
• Authors and manages approval of Informed Consent Documents (ICDs) including responses to external stakeholder questions
• Reviews and approves final document and Risk Management and Safety Review Plan

Clinical Development Scientist – Director

• Responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio
• Clinical development expert for assigned studies maintaining current scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment
• Effectively partner with other clinical and medical colleagues, clinical operations and other functional lines for the successful implementation and execution of the clinical trial(s) within the assigned program
• Represent the study team in governance meetings and submissions, partners with/supports the Development lead/Medical Director regarding study and disease area strategy
• Author protocols, study level informed consent documents, and contribute to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents
• Set the clinical data review strategy and lead the team in the collection of quality data and review of emerging clinical data and trends

Oncology Late Stage Clinical Development Scientist – Non MD, Director

Data Scientist

• Serves as Clinical Data Scientist and Trial Lead for one or more clinical trials assuming responsibility for all CDIS activities including selection and application of data acquisition standards, Data Management Plan, selection of quality risk indicators, third party study data due diligence.
• May functionally manage a team of Associate Data Managers, Senior Data Managers, be responsible for resource allocation, training and development.
• Works with Asset Leads to establish strategy, timelines, and adequate resourcing of DMs at Asset/Study level.
• Ensures appropriate documentation across the lifespan of the study/asset for all DM deliverables and ensures the required study specific CDIS documents in the Trial Master File (TMF) are of high quality and are filed contemporaneously.
• May likely be involved in development of TA specific standards.
• Provides project management leadership to DM teams – Responsible for managing issues at the study level as they arise and proactively communicating to Asset Lead and Management while serving to provide solutions.
• Acts as the key scientific and technical data management expert; contribute to department level initiatives and ensure effective reporting of study status and metrics to Management.
• Ensures work carried out on behalf of CDIS is in accordance with applicable SOPs and working practices.
• Serves as Subject Matter Expert (SME) for and oversees the design, documentation, testing and implementation of clinical data collection tools, both CRF and non-CRFs using and electronic data capture (EDC) system and/or other data collection systems.
• May act as data management contact for regulatory inspections/audits in liaison with the appropriate Quality and Safety groups with Pfizer.