Pfizer

Accounts Receivable

• Drives sales in assigned territory
• Engages with customers both face to face and virtually
• Develops and implements effective business and territory call plans
• Effectively builds rapport and relationships with customers in both live and virtual environments
• Understands and leverages internal reports and analytics to assist with identifying, developing, and implementing strategic business opportunities
• Collaborates effectively and compliantly across the organization to address customer inquiries and advance Pfizer objectives

Cardiovascular Specialist

Business Operations

• Formalizing the strategy, processes, communications, and systems to maximize CFC engagement
• Collaboratively improve the sales effectiveness of CFCs
• Identify issues impacting organizational goals and solutions
• Lead and manage critical projects advancing organizational effectiveness
• Evolve and manage selling skills and capability curriculum for CFCs
• Collaborate with US Marketing Teams, Training, and Sales leadership

Operations Manager – Business Operations/Enablement, Vaccines Sales

Supervisor

• Quality Assurance & Inspections and Internal Audit
• Local Product Disposition & Resolution of Product Quality
• Supplier Quality Management
• Leadership Skills
• Local Requirements

Supply Operation Quality Supervisor

Research Analyst

• Independently manage and monitor assigned investigator sites from initiation to database lock.
• Ensure compliance with Study Monitoring Plans, SOPs, GCP guidelines, and prevailing laws.
• Partner with Site Care Partners prior to site activation on crucial feasibility and site selection processes, Pre-Trial Assessments (PTAs), site activation checklists, Informed Consent Document (ICD) finalization, and Site Initiation Visits (SIVs).
• Actively mentor and train Clinical Research Associates (CRAs) as assigned, supporting their development and operational capability.
• Serve as a Subject Matter Expert (SME) for CRA-related processes and participate in regional or local working groups and process improvement initiatives.
• Identify, resolve, and manage complex investigator site issues.
• Establish and implement robust CAPAs, manage Quality Event remediations, support sponsor regulatory interactions/inspections, and drive Audit Observation CAPA developments.
• Partner with SCPs, Country SOMs, Clinicians, Recruitment Specialists, and Clinical Data Scientists.
• Monitor site-level AEs/SAEs, collaborate with the Drug Safety Unit, handle investigational product oversight (accounting, storage, destruction), support database release, and conduct co-monitoring activities as requested.

Senior Clinical Research Associate I

• Coordinate and support clinical trial activities, assisting managers in their execution.
• Contribute to project tasks and milestones, organizing work to meet deadlines.
• Work in a structured environment using established procedures, seeking guidance from colleagues.
• Maintain the Pfizer Trial Master File (PTMF) in compliance with ICH-GCP and SOPs, and ensure team members update tracking and files as needed.
• Timely update trial and site information in the Corporate Clinical Trial Registry and support Clinical Trial Applications to ethics committees and regulatory authorities.
• Provide administrative support for protocols and Informed Consent Documents (ICD) to global Project Managers and Study Managers, assisting with activities within set timelines.
• Develop and maintain local tracking spreadsheets for study-related documents, data, and activities, prepare supportive materials for sites, attend training programs, and identify process improvements for inspection readiness and PTMF compliance.

Clinical Research Associate, CRA

• Drives sales in assigned territory
• 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 to appropriately educate providers on unbranded and branded product value proposition for relevant patient populations and effectively and strategically utilizes approved clinically oriented disease state information and patient resources, as applicable
• Demonstrates strong teamwork capabilities to collaborate effectively and compliantly across the organization to address customer inquiries and advance Pfizer objectives
• Completes all administrative expectations on time and compliantly.

Compliance

• Accountable for investigation of quality issues related to Laboratory investigations
• Responsible for deviation investigation and out-of-specification and atypical result investigation
• Reviews protocols, analytical results and/or documents associated with investigations
• Conducting laboratory investigations (LIR/ RAAC/ Incident and QAR) through eQMS
• Initiation of Corrective and Preventive actions related to LIR/ RAAC/ QAR
• On time submissions of LIR/ RAAC/ Incident and QAR for closure
• Preparing Annual Trend for Laboratory Investigations
• Ensuring the accuracy of the Analytical data prior to closure of investigations
• Coordinate with the CFTs for closure of investigations
• Tracking and on time closure of action items

Associate Manager – BQ QMS & Compliance

SEO Marketing

• Provides strategic & operational leadership for QSEO digital portfolios and digital capital projects
• Drives governance, prioritization, and lifecycle tracking across initiatives
• Partners with business process owners and digital product owners to enable transformation and operational excellence
• Accountable for Digital project intake, endorsement, deployment planning, communication, value tracking
• Facilitates QSEO digital program in partnership with the respective GPO and Digital creation center lead
• Coordinates annual Digital budget planning and endorsement
• Implements and maintains QSEO digital portfolio management framework
• Aligns business process owners and digital product owners to portfolio priorities and execution plans
• Develops, communicates and monitors Digital deployment plans
• Implements holistic program and portfolio management tooling with PGS process alignment
• Leverages AI to expedite the portfolio management process
• Supports development of QSEO Digital assessments and business case development
• Ensures adherence to scope, schedule, and quality standards across all initiatives
• Facilitates governance forums for intake triage, investment decisions and prioritization
• Monitors portfolio health, risks, and performance metrics to optimize resource allocation
• Defines and communicates RACI and decision-making improvements

Digital Portfolio Lead

Product Manager

• Lead the development of AI and data-driven digital products through iterative, value-focused delivery approaches to validate concepts and accelerate time-to value.
• Define and communicate a clear product vision and strategy that prioritizes speed, experimentation, and learning through iterative delivery.
• Collaborate closely with cross-functional teams—including engineering, design, and business stakeholders—to quickly test hypotheses and refine product direction based on user feedback and data.
• Establish and manage a lean product roadmap focused on delivering high-impact features with minimal viable scope, while maintaining flexibility to pivot based on insights.
• Drive agile ceremonies and sprint planning with a focus on short cycles, fast feedback loops, and continuous improvement.
• Champion a culture of experimentation, encouraging A/B testing, user research, and analytics to inform product decisions.
• Ensure solutions are scalable and extensible, laying the groundwork for future enhancements while meeting immediate business needs.
• Lead the creation of user stories, solution designs, and wireframes that reflect user-centric design principles and solve real-world problems.
• Manage stakeholder expectations by clearly communicating trade-offs, timelines, and outcomes of solution launches.
• Foster a team environment that embraces ambiguity, adapts quickly to change, and thrives on delivering tangible results in compressed timeframes.

Director, Product Lead

Financial Planning and Analysis

• Lead planning and completion of BFC deliverables
• Provide metrics and insights for planning and decision-making
• Serve as point of contact for Local Finance colleagues
• Build relationships within Local Finance Teams
• Handle urgent requests within timelines

Senior Business Finance Centre Partner – 6 month Secondment

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

• 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.

Cardiovascular Specialist

Operations Manager – Business Operations/Enablement, Vaccines Sales

Supply Operation Quality Supervisor

Senior Clinical Research Associate I

Clinical Research Associate, CRA

Cardiovascular Specialist

Associate Manager – BQ QMS & Compliance

Digital Portfolio Lead

Director, Product Lead

Senior Business Finance Centre Partner – 6 month Secondment

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