Pfizer

Medical Director

• Provide Clinical Development leadership and expertise on clinical trials
• Oversee design, conduct, and analysis within the PF 4404 program
• Collaborate with other functions such as regulatory affairs, pharmacovigilance, and medical affairs
• Conduct medical monitoring activities including eligibility assessment and safety monitoring
• Lead peer-to-peer interactions with investigators
• Serve as the point of contact for clinical issues
• Lead development and maintenance of clinical trial and regulatory documents
• Collaborate to review and interpret clinical data with key findings

Clinical Development Medical Director, Oncology

Support Engineer

• Monitor and evaluate Customer Service Representatives' interactions via phone and email with health care professionals, consumers, distributors, pharmacies, and other stakeholders against established metrics
• Provide coaching and feedback from these evaluations to team members and supervisors
• Review our strategies and team efficiency to effectively manage planned and unplanned events
• Conduct on-boarding orientations for new hires
• Provide comprehensive ongoing training for all levels of Customer Service
• Create and maintain metrics to develop necessary training and ensure program success
• Collaborate with the management team to analyze practices and procedures
• Assist workforce analysis, promoting consistency, best practices, and tactical guidance
• Design, perform, train and distribute routine reports required by management
• Assist in creating training documents for managing day-to-day tasks and work on streamlining SOM processes and communications.

Customer Service Support Analyst

Supply Chain

• Lead and manage matrix teams responsible for end-to-end oversight of supply chain activities for clinical studies.
• Provide consultation on investigational product strategies and sourcing strategies.
• Design strategies that align with program, protocol, and regulatory requirements.
• Manage multi-million clinical supply budgets and provide guidance to the Clinical Supply Team (CST).
• Identify potential risks and develop supply strategies to mitigate risks and create contingency plans.
• Act as a point of contact for clinical supply required input during audits and regulatory inspections.

Manager, Supply Chain Lead

Risk

• Acts as a Safety point of contact for the Asset Teams and chairs the Risk Management Committees (RMCs)
• Oversees proactive safety surveillance and risk management to effect product safety signal detection & evaluation
• Represents Pfizer WWS at internal and external forums as appropriate
• Evaluates safety data, identifies and analyzes safety signals, and presents medical evaluation of safety signals
• Prepares action plans independently to address risk and benefit-risk issues
• Ensures consistency of safety risk messaging across multiple indications/BUs

Director, Safety Risk Lead

Director

• Act as Clinical Pharmacology representative on Clinical Sub Team and Development Team and other multifunctional teams as appropriate
• Responsible for providing expertise, leadership, and deliverables of clinical pharmacology for the assigned projects within sphere of influence
• Design and execute clinical pharmacology plans and implement clinical pharmacology best practices on project teams
• Work closely with other disciplines to ensure that sufficient preclinical PK/PD knowledge exists to underwrite safe human administration and to establish the structure of a predictive model prior to FIH
• Responsible for planning and overseeing clinical pharmacology aspects at the project level (e.g clinical development plan, implementation and interpretation of PK/PD analyses, PK/immunogenicity/biomarker measurement strategies etc.)
• Plan and oversee study level activities including protocol authoring, clinical phase oversight, and reporting
• Responsible (with clinicians and statisticians) for ensuring appropriate dose-range finding strategies which ultimately will lead to optimal doses and dosage regimens in patients
• Accountable for ensuring appropriate design and implementation of End-to-End MIDD plan that conforms with best practices
• Responsible for ensuring use of innovative analytical methods to integrate knowledge of PK, PD, patient characteristics and disease states to optimize doses, dosage regimens and study designs
• Provide End-to-End clinical pharmacology contribution to regulatory documents (e.g., Briefing documents, Regulatory queries, Investigator’s Brochures, IND, NDA/MAA, etc.)
• Develop new methodologies through internal and/or external collaborations with world leading experts
• Coach less experienced colleagues and team members
• Stay abreast of literature, regulatory guidelines, and internal guidance and SOPs
• Influence external environment through publications, presentations, and representation at scientific societies and industrial consortium

Associate Director, Clinical Pharmacology Lead

Product Manager

• Define and evolve the AMP product vision, multi‑year roadmap, and success metrics
• Translate strategic objectives into prioritized, outcomes-driven product capabilities
• Manage 3 - 4 AMP product owners and guide cross-functional Design/Build pods
• Establish and maintain product governance
• Oversee delivery from early concepts and alpha prototypes
• Translate business and user requirements into actionable product features
• Ensure transparency into product performance through data driven‑ metrics
• Collaborate with business, engagement, and operations leaders to incorporate user feedback

End-to-End Product Lead, AMP

• Support the development of the roadmap for the AMP product portfolio
• Translate business priorities into scalable product capabilities
• Collaborate with development teams and international stakeholders
• Ensure alignment across the marketing and technology ecosystem
• Drive execution excellence from concept to enterprise-wide adoption
• Manage product governance and ensure transparency through data metrics

Product Owner, AMP

Sales

• Responsible for launching new products and managing business relationships.
• Engage in product promotion within assigned accounts.
• Build rapport and relationships with customers across virtual and F2F environments.
• Utilize current digital tools effectively for customer engagement.
• Provide insights for the development of new product messaging.

Gastroenterology Health & Science Sales Specialist - Pasadena / Inland Empire, CA

Compliance

• Provide regulatory guidance and strategic support for review of promotional communications
• Ensure compliance with regulatory standards and internal policies
• Interact with OPDP/APLB on routine matters
• Mentor and provide guidance to junior personnel
• Review and advise on promotional communications
• Identify potential regulatory risks and propose mitigation strategies
• Represent US RAP perspective in review team meetings

Manager, US Regulatory Advertising, Promotion

Customer Success Manager

• Collaborates with a wide range of stakeholders to gather customer insights and develop patient-focused solutions.
• Accelerates and optimizes customer engagement that drives incremental value for the customer, Pfizer and the patient within the IAT process.
• Works closely with marketing colleagues and agency partners to help drive solutions that support mutually aligned goals for the customer and Pfizer.
• Develops an optimal plan for effectively implementing, communicating, and improving patient care aligned with appropriate goals and KPIs.
• Contributes to the overall operational excellence of I&I engagement with key accounts.

Advanced Customer Engagement Director – Central

Artificial Intelligence

• Drive scientific and technical advancement in PDM’s AI and cheminformatics capabilities by developing and delivering robust, validated workflows and algorithms that directly support drug discovery.
• Design, build, and deploy innovative cheminformatics and AI workflows for small molecule discovery, with clear deliverables including prioritized compound lists, well-defined chemical libraries, and actionable structure-activity relationship analyses.
• Collaborate closely with medicinal chemists, biologists, and data scientists to integrate computational approaches into experimental and analytical workflows.
• Continuously monitor and evaluate emerging advances in AI, cheminformatics, and computational drug discovery, proactively leading the adoption of promising new methodologies.
• Develop novel algorithms and analytical strategies tailored to Pfizer’s proprietary datasets and key scientific questions, with measurable outcomes such as validated models, software tools, and contributions to scientific literature or patent filings.

Senior Principal AI/ML Cheminformatics Scientist

• Responsible for the supervision and leadership of Retail Pharmacy Account Manager (RAM)
• Manage retail pharmacy business performance and deployment of sales and marketing strategies
• Coach the account team to build productive relationships with retail pharmacy field leaders
• Collaborate with HQ and across Pfizer
• Develop a business plan reflective of market dynamics, brand priorities, and alignment across the specific retailer footprint
• Monitor performance and adapt strategic plans to achieve the business potential
• Engage with cross-functional teams to execute on opportunities for brand Operationalization

National Pharmacy Business Director – Walmart/Sam’s Club/Costco

• Develop and evaluate product-, portfolio-, and channel-level contract strategies for assigned institutional customer segments
• Own contract strategy for designated high-complexity accounts, supporting negotiations and implementation in partnership with cross-functional teams
• Lead the design and refinement of contracting programs and pricing approaches responsive to market dynamics and customer needs
• Collaborate with internal stakeholders to identify compliant and implementable contracting solutions aligned with business strategy
• Analyze internal and external data to support contract strategy development, negotiation preparation, and portfolio assessments
• Evaluate contract performance, customer behavior, and financial impact across contracting scenarios
• Apply knowledge of institutional customers and pharmaceutical distribution channels to inform contracting strategies
• Ensure contract strategies comply with legal, regulatory, and company policy requirements

Director, Contract Strategy

Operations

• Provide Business facing OE Support to ES Clusters and/or PC1
• Drive the ES Clusters/PC1 Governance in alignment with IMEx
• Be a central part of the ES Clusters/PC1 and a facilitator as needed of the weekly, monthly and quarterly cadence of team meetings
• Facilitate/Co-lead the ES Cluster/PC1 Strategy and Goal setting
• Lead/Support/Coach OE solutions in the ES Clusters/PC1 e.g. Continuous Improvement Loop, IMEx Deployment, Innovation, Agile Transformation, Complex Investigations in alignment with the ES/OE Strategies
• Lead/Coach the CI Process within the ES Clusters / PC1 at T4 VSLT and T3/T2 VSOT/VPT levels
• Lead/Support/Coach the deployment of ES OS solutions e.g. Continuous Improvement Loop, IMEx Deployment, Agile Transformation, EIRM, facilitate Innovations Workshops at the BU level
• Coach Complex Investigations using the established process
• Work with the ES OE team to ensure appropriate skills are deployed by BU and region
• Build OE & Innovation capabilities at the ES Clusters/PC1 and selected CMOs
• Build M1, M2, M3, M4, PHP and Innovation capabilities within the ES Cluster/PC1 in conjunction with the PGS OE Teams
• Embed CI mindsets & behaviors in the BU team and supporting functions
• Contribute to the OE & ES Strategies
• Assist with co-design of OE programs
• Facilitate ES S&OE team meetings

Operational Excellence Lead

• Develops and executes PCOA strategies to support therapeutic area/asset specific clinical development plans, global HV&E strategies, integrated evidence plans, and commercial strategies.
• Effectively collaborates with cross-functional stakeholders to ensure that the PCOA strategies and related deliverables are fit-for-purpose and aligned with the overall program goals.
• Ensures that PCOA strategies are aligned with the most current regulatory and HTA guidance documents (e.g., FDA, EMA, JCA).
• Leads qualitative and quantitative evidence generation research to inform and support PCOA strategies.
• Provides technical expertise in the implementation, analysis, interpretation, and communication of clinical outcome assessment (COA) data.
• Manages a global network of consultants and contract organizations to execute the COA evidence generation deliverables (e.g., qualitative COA development evidence, psychometric analyses, COA qualification dossiers).
• Maintains awareness of new research methods, tools, and data sources to ensure study methods represent current state of the science.
• Promotes the value of patient-centered outcome assessments across Pfizer through education and training.