Pfizer

Data Engineer

• Build and prototype AI enabled solutions supporting Oncology R&D workflows and decision making
• Develop and maintain data pipelines, feature engineering workflows, and analytical models
• Apply machine learning techniques to structured and unstructured healthcare data
• Collaborate with scientific and product partners to understand needs and deliver usable tools
• Focus on speed, iteration, and usability, with production scaling supported by enterprise Digital teams as appropriate
• Contribute to shared engineering standards, documentation, and best practices.

Senior Manager, AI and Data Engineering

Full-stack Engineer

• Own the Oncology AI product strategy and roadmap across discovery, translational science, clinical development, and real-world evidence.
• Lead and manage a cross functional team of AI engineers, providing technical direction, prioritization, and coaching.
• Translate complex scientific and operational problems into clear AI product requirements, success metrics, and delivery plans.
• Partner with Oncology scientific leaders, clinical teams, Digital, Enterprise AI, and IT to ensure solutions are aligned with enterprise platforms and governance.
• Evaluate AI concepts, prototypes, and technical approaches, providing informed guidance and trade‑off decisions.
• Assess Oncology workflows to identify and propose opportunities for automation and process improvements.
• Drive stakeholder engagement, change management, and adoption, ensuring AI solutions move beyond pilots to sustained impact.
• Establish lightweight governance, delivery standards, and value tracking for Oncology AI initiatives.
• Represent Oncology AI initiatives in leadership forums and cross-enterprise discussions.

Director, Oncology AI Product – Engineering Lead

Manager

• Own the development and execution of the Prevnar 20 HCP strategy and tactical plan
• Drive the pull through of HCP tactics for Prevnar 20 Pediatric
• Develop, deliver, and measure marketing solutions that differentiate Prevnar 20 Pediatric with HCPs
• Assess digital metrics, insights and make recommendations for content and channel optimization
• Engage with sales and account management leads to solicit insights and provide solutions
• Develop training resources for use with CFCs
• Manage promotional budget for tactics owned

Senior Manager – Pediatric

Data Scientist

• Serves as Clinical Data Scientist and Trial Lead for one or more clinical trials
• Responsible for all CDIS activities including selection and application of data acquisition standards
• May functionally manage a team of Associate Data Managers, Senior Data Managers
• Works with Asset Leads to establish strategy, timelines, and adequate resourcing of DMs
• Ensures appropriate documentation across the lifespan of the study/asset for all DM deliverables
• Provides project management leadership to DM teams
• Acts as the key scientific and technical data management expert
• Serves as Subject Matter Expert (SME) for and oversees the design, documentation, testing and implementation of clinical data collection tools.
• May act as data management contact for regulatory inspections/audits in liaison with the appropriate Quality and Safety groups.

Senior Clinical Data Scientist

Content Marketing Manager

• Developing global medical 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 under supervision.
• Researching, organizing, compiling, interpreting, and quality check of 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 and Content Solutions – Vaccines

Account Executive

• Develop, maintain and grow strategic long-term HCPs, SPPs, Alternate Site, PBMs/Plans and Key Stakeholders customer relationships
• Develop and execute customer business plans
• Manage HCPs, SPPs, PMBs, Plans and customer contracts
• Conduct monthly business reviews with assigned accounts

Key Account Director

Chief Marketing Officer

• Own pre-launch and launch readiness for Dazukibart, ensuring robust strategy across: Patient journey and funnel development, Segmentation and targeting, Scientific narrative and value story, Omnichannel engagement strategy, Positioning and Marketing Campaign Development
• Lead market shaping strategy for Dermatomyositis, including HCP and Patient Market Research, disease education, unmet need articulation, diagnostic journey optimization, and stakeholder engagement.
• Lead Octagam HCP and Consumer marketing efforts, working collaboratively with Ig Marketing Lead, MLR, GCET, IIS, CMO and Agency.
• Support marketing efforts for Panzyga, ensuring portfolio cohesion and strong performance and growth
• Coordinate efforts and ensure alignment with Ig Marketing Lead
• Partner closely with MLR, Market Access, Sales, GCET, and IIS to ensure launch excellence and organizational readiness.
• Establish clear success metrics and insight loops to guide decision-making pre-and post-launch.
• Ensure seamless interaction between current Octagam DM performance and future launch planning, protecting performance while building the category.
• Lead development and approval of promotional materials, campaigns, and field tools in compliance with GCMA and RC requirements.
• Collaborate with field leadership to ensure strong field execution against the portfolio goals and POA excellence.

Ig Dermatomyositis Marketing Director – Launch Lead

• The successful candidate is expected to carry out the functions of the BA-DS team, which are rooted in translating key commercial business questions into advanced analytic insights.
• Strong emphasis is placed on applying data science principles to the business problem, rigorously documenting the end-to-end analytic pipeline, purposely communicating with stakeholders, and delivering effective presentations appropriate to the target audience.
• The secondment is focused – but not limited – to high-impact workstreams that are anchored around two core capabilities of the BA-DS team – Dynamic Targeting and Dynamic Content.
• These workstreams provide the opportunity to leverage technical leadership in building and optimizing data models and processes, while also collaborating with Commercial and GCA stakeholders. Other projects may also be prioritized given specific needs and timelines.

Director, Business Aligned Data Science – Secondment, 6 Months

Medical Director

• Plan and execute Medical strategy and engagement for assigned customers 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 customer insights
• Deliver approved medical content about Pfizer medicines and relevant topics in the designated therapeutic area
• Cultivate research and therapeutic area expertise, including familiarity with latest congress data and disease state literature

Prostate Field Medical Director – Non-MD

Security Engineer

• Own and drive the strategic vision for Identity Security and Access Management across the organization, aligning ISAM initiatives with broader cybersecurity and business objectives
• Develop and manage the ISAM budget, ensuring alignment with organizational goals and effective allocation of resources
• Monitor expenditures, forecast future budget needs and identify opportunities for cost optimization
• Lead the transformation of legacy identity management systems and deliver on a multi-year modernization roadmap, including the enterprise-wide implementation of SailPoint
• Champion the adoption of modern ISAM practices and technologies, including Ping Identity, ensuring scalable, secure, and future-ready solutions
• Take ownership of Privileged Access Management, ensuring seamless integration with existing ISAM systems while maintaining operational excellence and legacy support
• Oversee directory services and certificate management processes, ensuring they are secure, available, efficient, and aligned with enterprise standards across a global environment
• Define and execute strategies to enhance identity governance controls, including access request, provisioning, and de-provisioning, with a focus on automation and user experience
• Drive enterprise-wide strategy and execution for MFA, SSO, and Federation services, ensuring secure and seamless authentication across internal and external platforms
• Define and implement identity and access entitlement frameworks, ensuring granular access control aligned with business roles and regulatory requirements
• Ensure integration and interoperability across ISAM capabilities, including PAM, directory services, certificate management, and federated identity, to support a unified and scalable ISAM architecture
• Ensure compliance with internal and external audit requirements, maintaining a high level of security and operational resilience in ISAM systems
• Collaborate with cross-functional teams to ensure ISAM requirements are embedded into the organization’s security architecture and technology strategy
• Lead and mentor a multi-national team through complex ISAM projects, providing clear direction, accountability, and support to deliver high-impact outcomes
• Act as a trusted advisor to senior leadership, translating technical ISAM concepts into strategic business value and influencing decision-making at the executive level.

Senior Director, Identity Security and Access Management

Director

• Plan and execute independent Medical strategies for external medical stakeholders
• Maintain knowledge of relevant TA/disease states and provide therapeutic area/product information
• Serve as a conduit for Medical Information and external medical stakeholder insights
• Educate external medical stakeholders based on patient care gaps
• Deliver approved medical content about Pfizer medicines

Director, Specialty Care Field Medical

• Provide therapeutic area/product expertise for the designated therapeutic area across a broad range of external medical stakeholders
• Plan and execute independent Medical strategies and engagements for assigned external medical stakeholders
• Maintain required level of knowledge of relevant TA/disease states
• Serve as a conduit and resource for Medical Information and external medical stakeholder insights
• Optimize patient care improvement in Medical communications and deliverables
• Deliver approved medical content about Pfizer medicines and relevant topics in the designated therapeutic area
• Collaborate with US and/or Global Medical Affairs colleagues
• Mentorship – Onboarding partner, ad board, and study lead mentor

Specialty Care Field Medical Director, MD

• Own hands‑on delivery, operationalization, and continuous improvement of one or more core Evidence Generation systems
• Lead strategically important cross‑system capabilities spanning multiple interdependent Evidence Generation systems and external dependencies
• Translate end‑to‑end Evidence Generation business priorities and roadmap intents into aligned functional requirements, system designs, and integration approaches across systems
• Ensure delivery aligns with roadmap priorities and business outcomes
• Lead and orchestrate system‑level and cross‑system integrations and dependencies
• Define and execute system‑level and cross‑system training, user enablement, and communication strategies
• Act as a senior system owner and escalation point for issue resolution
• Execute assigned roadmap initiatives, proactively managing dependencies, sequencing, and delivery risks
• Work closely with cross‑functional stakeholders to ensure solutions are strategically aligned, operationally fit, and compliant

Director, Evidence Generation Systems

• Independently leads clinical execution of one or more studies; accountable for program level clinical deliverables
• Provides input to the protocol design document; leads development of the protocol, including protocol amendments
• Represents the study team in internal protocol review governance submissions and interactions
• Ensures development of Study Informed Consent Documents
• Provides clinical guidance to the development of the Statistical Analysis Plan
• Sets the clinical data review strategy and leads the team in the review of emerging clinical data and trends
• Develops site selection criteria
• Serves as the primary clinical point of contact with investigators and study team
• Ensures TMF compliance for clinical documents
• Leads the adoption and implementation of continuous improvement activities

Senior Clinical Development Scientist

• Accountable for safety across the study: Provide study team with medical advice for all medical issues during risk assessment and mitigation planning to enable quality, compliance and patient safety at trial, site and patient level.
• Ensure development of and adherence to the Safety Surveillance Review Plan (SSRP).
• Monitor study safety issues and provide input to serious adverse events (SAEs) reports.
• Provide appropriate medical context in terms of risk factors, medical history and other important medical factors required to put the SAE or AE into appropriate medical context.
• Participate in the Safety Review Team to evaluate medical benefits/risks to support targeted clinical indications.