Pfizer

Manager

• Assist in and/or lead negotiations for Federal Supply Schedule (FSS) contract
• Fulfill regulatory requirements for contract administration processes
• Develop contract proposals and agreements that maximize product utilization and profitability
• Present recommendations to upper management for approval
• Administer the executed agreement and manage contracts during their term
• Collaborate with internal stakeholders to develop the annual operating budget and quarterly accrual/formulary tracking updates

Manager – Government Contracts

Analytics Engineer

• Build scalable data pipelines to provide accurate and impactful business analytics and insights
• Design and implementation of data architecture and infrastructure
• Lead the development of data management strategies and policies
• Manage a team of project data engineers and analysts
• Ensure data quality and integrity across all data platforms
• Collaborate with cross-functional teams
• Develop and maintain data governance frameworks
• Oversee the integration of new data technologies and tools
• Drive the optimization of data processing workflows and pipelines
• Lead the development of analytics solutions to support business decision-making
• Manage relationships with external data vendors and partners

Manager, Data and Analytics Engineer

Director

• Responsibility for site management and monitoring activities in Germany
• Functional and disciplinary leadership, including coaching of CRAs and other monitoring roles
• Ensuring quality, compliance and patient safety in accordance with GCP, regulatory requirements and internal standards
• Close collaboration with Study Start-Up, Regulatory, Medical Affairs, CROs and other internal and external partners
• Contributing to the development of country and site strategies

Director, Site Management – Monitoring

• Build scalable data pipelines
• Design and implement data architecture and infrastructure
• Implement data management strategies and policies
• Ensure data quality and integrity
• Collaborate with cross-functional teams
• Develop data governance frameworks
• Integrate new data technologies
• Ensure compliance with data privacy regulations
• Optimize data processing workflows
• Develop analytics solutions for business decision-making
• Maintain relationships with external data vendors
• Create and maintain data documentation
• Develop and monitor key performance indicators

Senior Associate – Data and Analytics Engineer

• Deliver data driven-insights & solutions for patient services programs for Pfizer’s (Oncology / Primary Care) business unit
• Partner with functional leads for Pfizer’s Business Analytics community, Pfizer Business Technology, the Specialty Pharmacy Provider (SPP) center of excellence and external SPP customer, legal and compliance to develop and implement models, insights, and data products that drive each brands’ strategic priorities
• Represent PPS Patient Solution Insights & Analytics Leadership, as the subject matter expert, to build data-driven alignment on program strategy decisions for brand leaders
• Perform sophisticated syntheses across multiple insight sources (i.e., secondary analytics, primary strategy, and stakeholder feedback) to deliver impactful and relevant patient services strategy recommendations
• Identify KPIs to monitor and diagnose program performance and operational execution, across the patient journey
• Maintain data governance standards to ensure consistency and clarity in program metrics / business rule implementation over time
• Proactively work across the enterprise to push novel analytic methodologies, co-create solutions and oversee implementation of solutions with stakeholders
• Identify efficiencies and future-forward ways to accelerate the timeliness of analytics / insights delivery
• Work within a high-performing team of insights professionals, responsible for delivering integrated insights, program measurement analytics, reporting, and launch support for each BU
• Partner with PPS cross-functional teams, Digital, Operations, Access / Affordability, and Patient Assistance Programs to pull through insights into action plans
• Monitor and manage research and analytics program budgets, identifying opportunities for cost savings, and ensuring financial compliance

Director, Patient Solution Insights & Analytics

Communications

• Lead Oncology scientific communications strategy and execution for assigned Pfizer programs
• Develop and lead integrated scientific communications strategies aligned with Oncology Medical TA priorities
• Partner with Global Product Teams to support external engagement around key clinical trial data readouts
• Ensure alignment of product-level scientific communications with medical priorities through cross-functional collaboration
• Serve as a strategic thought partner to TA Medical teams
• Manage planning, forecasting, and budgets for scientific communications deliverables
• Collaborate with International Medical Channel Content teams for global asset sharing
• Maintain deep therapeutic area knowledge across inline and pipeline assets

Director, Oncology Scientific Communications – Therapeutic Area Lead

• Engage with healthcare professionals and other stakeholders to generate insights that inform medical strategy
• Help shape, implement, and continuously improve Medical Insights processes
• Partner closely with Medical Engagement & Impact (MEI), US Medical Affairs, Digital & Technology, Medical Systems
• Maximize the value and impact of Medical Insights by embedding them into strategic discussions and decision‑making
• Contribute to the development and evolution of Medical Insights strategies and frameworks
• Drive alignment of Medical Insights approaches across Medical Affairs
• Identify and prioritize opportunities across the end‑to‑end Medical Insights lifecycle
• Define and monitor indicators of value and impact to assess how insights inform Medical decisions

Director, Medical Insights

Outside Sales

• Independent management of relationships with medical professionals in hospitals
• Primary point of contact for the innovative oncology portfolio
• Identify stakeholder interests and collaboratively develop patient-focused solutions
• Communicate and exchange scientific information in compliance with legal and regulatory requirements
• Contribute significantly to improving treatment outcomes by providing training and services to relevant stakeholders

Pharmaceutical Field Representative – Oncology

Compliance

• Provide regulatory guidance and strategic support for promotional communications
• Review and advise on promotional communications ensuring compliance with regulations and policies
• Identify potential regulatory risks and propose strategies to address/mitigate
• Represent US RAP perspective in cross-functional review team meetings
• Interact with OPDP/APLB staff on administrative and logistical issues

Manager, US Regulatory Advertising and Promotion

Content Marketing Manager

• Develop relevant medical affairs content, including abstracts, manuscripts, congress posters/presentations, graphical abstracts, systematic literature reviews, plain language summaries, slide decks, medical education resources, social media, infographics, video, multi-media and other types of external-facing medical content
• Research, organize, compile, interpret, and quality check various types of technical and/or medical content
• Provide solutions to stakeholders in alignment with manager for all projects and collaborate with other teams to drive these solutions (Graphics, Compliance agency, Statistics teams, etc.)
• Ensure execution of all projects within expected timelines while adhering to all quality and compliance requirements for medical content
• Ensure training on relevant tools and processes, including new generative AI technology platforms, that ensure efficient and compliant execution of all medical affairs content
• Track the progress of projects and resolve any issues/problems with guidance from manager
• Identify and train to become an expert on one new tool/skill for content creation representing the latest trends in the industry

Associate Manager, Medical Communications, Content Solutions

Affiliate Manager

• Responsable du démarrage et de l’activation des centres.
• Procéder à la qualification et à l’activation des centres assignés.
• Appuyer les processus afin d’optimiser les activités de sélection des pays et des centres.
• Collaborer avec les intervenantes et intervenants clés pour fournir une orientation aux échelles régionale et nationale.
• Mener les activités de démarrage des études dans les centres.
• Veiller à la réalisation de toutes les activités de mise en route des centres.
• S’occuper du maintien des relations et de la supervision de la qualité opérationnelle des centres.

Partenaire responsable, centres d'étude clinique

Product Manager

• International CFC Reporting Product Lead— Coordinating with Global Commercial Analytics to create a single, governed International CFC Reporting product roadmap
• Enabling a seamless transition to the new CFC Engagement Platform (Lifescience Cloud) in 2026 and beyond
• Mobile Product Leadership (CFC messaging) leveraging the multi year mobile messaging strategy to optimize the channels (SMS, WhatsApp Business API)
• Drive AI assisted messaging and in app guidance
• Deliver operational excellence across U.S. and International portfolios
• Provide end to end product strategy, governance, investment prioritization, and operational delivery across both domains
• Lead cross-functional teams, working closely with CMO, Digital, Legal/Compliance, and local markets.

CFC Reporting & Mobile Product Lead – Director

Medical Director

• Accountable for the medical & scientific integrity of the study and the wellbeing of the patients enrolled in one or more clinical trials
• Apply technical and clinical/medical skills to ensure the design of efficient and high-quality clinical trials
• Responsible for effective execution of studies and works in close partnership with other clinical and medical colleagues
• Accountable for timely delivery of a quality protocol, clinical execution of one or more large and/or complex clinical trials
• Maintain compliance with internal and external standards, proactively mitigates risk

Director, Clinical Development – Medical Director, MD Required

• Overseeing the governance and operations of all enterprise-wide Patient Services vendor programs
• Ensuring all solutions are developed, maintained, and scaled in accordance with enterprise standards
• Collaborating cross-functionally to drive consistency and efficiency
• Facilitating relationships with third-party vendors who collect data or perform services
• Partnering with Digital and Analytics to develop strategies for acquiring data
• Executing optimal program design standards for scaling patient services across Pfizer’s portfolio
• Consulting and providing recommendations on organizational and operating models for patient services

Senior Manager, Patient Services Vendors – Hub Aff, e-Services

• Join the team that contributed to ending the COVID-19 pandemic.
• Structure and prioritize meeting feedback to distill highest value collaboration themes.
• Ideate around potential solutions to address consumer vaccination barriers while aligning to customer and Pfizer strategic priorities.
• Leverage data and analytics to size opportunity and quickly make resource and focus tradeoff decisions.
• Develop execution plan for aligned ideas and drive execution with a cross-functional ecosystem.
• Identify barriers to execution, problem solve, and escalate as needed to maintain forward progress.