Pfizer

Manager

• Act as Clinical Pharmacology representative on Clinical Sub Team, 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
• With some guidance, 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
• With some guidance, 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
• With some guidance, 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
• With some guidance, provide End-to-End clinical pharmacology contribution to regulatory documents (e.g., Briefing documents, Regulatory queries, Investigator’s Brochures, IND, NDA/MAA, etc.)
• Stay abreast of literature, regulatory guidelines, and internal guidances and SOPs
• Influence external environment through publications, presentations, and representation at scientific societies and industrial consortium.

Clinical Pharmacology Lead

Research Scientist

• Conduct comprehensive literature reviews and provide critical epidemiological insights
• Assess epidemiological data and literature to support disease contextualization and regulatory submissions
• Oversee epidemiological work with external vendors for literature reviews and regulatory deliverables
• Design and implement innovative database studies to quantify risks
• Conduct post-approval safety studies and develop strategies to address safety signals
• Engage with regulatory agencies on safety epidemiologic issues and participate in Risk Management Committee activities

Associate Director, Safety Surveillance Research Scientist

• Interact and successfully influence EVP/SVP internally, along with Senior Partners and CEOs of technology companies.
• Develop and deliver a comprehensive technology strategy that aligns with changing business needs, while leveraging the latest and emerging solution sets.
• Oversee SAP project planning, implementation, and management, including migrations to Cloud, upgrades, and integrations.
• Develop and execute a forward-thinking strategy for process transformation and innovation within functions.
• Develop and execute the solutions strategy that enables every Core function and Enabling function in Pfizer to deliver against their budget savings.
• Align transformation initiatives with the organization's long-term goals and innovation roadmap.
• Foster a culture of agility, continuous improvement, and operational excellence across finance and supply chain.
• Lead a team of technology and industry process experts to design, develop, and deploy next-generation technologies.
• Foster a culture of innovation and continuous learning within the team.
• Lead and manage transformation projects aimed at optimizing business processes and enhancing efficiency.
• Identify opportunities for implementing next-generation technologies, including automation and AI, to revolutionize operations.
• Maintain the SAP system landscape, including installation, configuration, and ongoing maintenance.
• Manage the lifecycle of SAP systems, including upgrades, migrations, and decommissioning.
• Collaborate with platform teams to identify opportunities for technology innovation and ensure seamless SAP system operations.
• Implement best practices and industry standards to drive innovation and excellence.
• Collaborate with stakeholders to ensure process and technical changes are effectively communicated and adopted.
• Stay abreast of industry trends, emerging technologies, and best practices to maintain a competitive edge.
• Manage technology budgets and allocate resources effectively.
• Lead and mentor a team of functional and technical professionals, fostering a culture of excellence and continuous improvement.

Vice President, SAP and Enterprise Solutions

Director

• Provide strategic input into clinical trial designs
• Lead the development of the evidence generation strategy
• Lead the coordination of input from local country/regional teams
• Lead the design and execution of global HEOR studies
• Develop patient-reported outcomes strategy
• Partner with internal stakeholders to ensure appropriate customer-facing dissemination of HEOR materials
• Develop strategic partnerships and research collaborations with key external experts

Director, HTA, Value & Evidence – Internal Medicine Early Pipeline

• Lead the development of the evidence generation strategy for Obesity treatments
• Coordinate input from local country/regional teams on evidence needs
• Design and execute global HEOR studies
• Develop launch deliverables including global value dossiers and economic models
• Provide strategic input into clinical trial designs
• Partner with stakeholders to ensure dissemination of HEOR materials
• Develop strategic partnerships with external experts and organizations

Director, HTA, Value & Evidence – Obesity

• Responsible for scientific oversight, data integrity and quality of clinical trial(s)
• Partner with clinical and medical colleagues, clinical operations and other functional lines
• Author protocols, study level informed consent documents, and contributes 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 leads the team in the collection of quality data
• Analyze the emerging safety profile of the drug
• Follow relevant SOPs and regulations, seeks opportunities to further improve quality and efficiency of clinical procedures

Oncology 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 our Oncology portfolio
• Clinical development expert for assigned studies maintaining current scientific and clinical knowledge
• Effectively partner with other clinical and medical colleagues, clinical operations and other functional lines
• Author protocols, study level informed consent documents, and contributes to authoring of clinical and regulatory documents
• Set the clinical data review strategy and leads the team in the collection of quality data
• Analyze the emerging safety profile of the drug in partnership with medically qualified colleagues
• Seek opportunities to improve quality and efficiency of clinical procedures

Senior Manager, Oncology Clinical Development

Medical Director

• Provide Clinical Development leadership and expertise on Late phase clinical trials
• Oversee the design, conduct, and analysis within Hematology
• Collaborate with other functions such as regulatory affairs, pharmacovigilance, biostatistics, and medical affairs
• Provide medical expertise and guidance to the clinical operations team, investigators, and external stakeholders

Clinical Development Medical Director, Hematology

Full-stack Engineer

• Lead business testing workstream for defect correction and enhancement releases; including identification of risks to current studies, developing and contributing to execution of the testing plan.
• Lead impact assessments of system updates, enhancements and defect corrections on iView2 reports.
• Participate in enhancement, sprint and release scoping discussions to support system enhancements to meet clinical trial and business needs.
• Partner with applicable system Product Owners, Product Area Leads and Digital technical team to ensure business continuity during planned releases and unplanned outages.
• Serve as IT Business Continuity process owner.
• Partner closely with other IGOT Technical leads on Impala 2.0 system issue escalations, support strategies and issue resolution.
• Provide technical and customer facing insights during design review meetings, Digital consultations, audits and regulatory inspections.
• Lead the resolution of technical issues and oversee or participate in quality investigations related to Impala 2.0 in collaboration with other technical/Digital resources.
• Maintain and monitor Impala 2.0 data standards, quality, compliance, security and usage of IRT related entities that reside in the Innovative Technology data dictionary and contribute to the overall data strategy for Global Clinical Supply.
• Evaluate data requests related to IRT and propose/implement potential solutions.

IRT Technical Lead – Impala 2.0

• Plan and execute medical strategy and engagement for appropriate assigned customers 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 customer insights, providing requested information to HCPs as allowed by Pfizer guidance and sharing customer viewpoints with Pfizer as appropriate
• Understand the priorities of Pfizer Medical Affairs to contribute to medical content strategy development and execute aligned Field Medical tactics
• Maintain effective and appropriate communication and collaboration among headquarters medical colleagues and other Pfizer Field Medical colleagues
• Demonstrate expertise in 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 centricity of medical communications and deliverables, incorporating health literacy and cultural awareness principles to ensure that patients remain the ultimate focus
• Deliver approved medical content about Pfizer medicines and relevant topics in the designated therapeutic area
• Identify and seek medical engagement from priority customer segments in assigned TA
• Provide truthful, accurate, and scientifically supported information in response to direct unsolicited medical requests from HCPs in a manner that complies with all applicable Pfizer guidelines, policies, and procedures
• Field relevant inbound queries from HCPs via established triage process
• In collaboration with Global Medical Affairs colleagues, partner with Oncology 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
• Appropriately provide medical support throughout the Investigator Sponsored Research (ISR) process
• Cultivate research and TA 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 customers
• 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

Senior Manager – Oncology Field Medical

Sales Operations Manager

• Provide key support/leadership to Therapeutic Area Regional Business Directors/National Sales Director
• Continuously improve sales operational effectiveness and efficiency for customer-facing colleagues
• Collaborate with US Marketing teams on brand strategies and messaging
• Coordinate with CEP Enablement Directors for Oncology specific operations platform training
• Develop, deploy and leverage new technologies for improving customer engagement activities
• Manage effective implementation and utilization of new technologies impacting sales function

Sales Enablement Manager – Hematology

Customer Success Manager

• Deliver world class, direct response strategies and tactics.
• Partner with product/brand marketing teams to translate their respective marketing objectives and strategies into the CRM channel strategy, including email, direct mail, and SMS among other channels.
• Blend creativity with data‑driven execution, leveraging segmentation, automation, and personalization to deliver impactful communications.
• Leverage AI tools to improve efficiency and efficacy to deliver omnichannel campaigns across paid, owned, and earned media.
• Drive CRM strategies and priorities to ensure success in developing deeper relationships with key targets for key brands.
• Collaborate with a broad range of commercial brand teams and cross-functional partners involved with the development, execution, analysis and actionable insights of CRM-related strategies and activities.
• Partner with marketing / commercial, Operations, MAR TECH and analytics teams to action on brand teams’ comprehensive strategy plan.

Senior Manager, CRM

• Drive GCP Quality by maintaining quality line-of-sight for assigned clinical trial programs
• Ensure program and study level quality oversight
• Monitor asset/study quality and identify risks and trends
• Provide study team Inspection Readiness guidance and support
• Oversee study-level quality risk management activities
• Represent quality functional lines at integration workshops and operational workshops

Asset Quality Lead – Director

• Driving CRM strategies and priorities to ensure success in developing deeper relationships with key targets for key brands
• Collaborating with a broad range of commercial brand teams and cross-functional partners involved with the development, execution, analysis and actionable insights of CRM-related strategies and activities
• Partnering with marketing / commercial, Operations, MAR TECH and analytics teams to: Action on each of the various brand teams’ comprehensive strategy plan to manage Pfizer interactions with targets across touchpoints, including campaigns, customer journey and omnichannel orchestration, personalization, and decisioning
• Defining the necessary data attributes and audiences for the CRM Personalization strategy and partnering cross-functionally to implement
• Leading the development of CRM program orchestrated contact targeting, reach and frequency strategies for sustained HCP engagement and ongoing Rx writing behavior changes
• Developing CRM learning agendas, measurement plans and segment level testing plans. Implementing tests, analyze results and present key insights and campaign optimization recommendations with key stakeholders
• Partnering with product/brand marketing, analytics, paid media, and digital to create data-driven omni-channel communication and experiences based upon the target’s individual needs
• Optimizing KPIs across journey planning, activation, measurement and optimization, including volumes and prescribing mix
• Applying scaled insights and CRM execution across the adoption path
• Identifying experience friction points across omnichannel journeys and assess where CRM can play a role to increase engagement, conversion and Lifetime Value (LTV)
• Auditing existing lifecycle content types & content quality to identify gaps and opportunities
• Developing CRM segment level content strategy, touch point message maps and creative briefs for CRM campaign programs
• Leading creative best practices for modular email design, SMS, MMS, Direct Mail, website CRM 1P & 0P data registration pages
• Initiating CRM campaign deployment requests, tag reporting meta data, track and manage campaign status via CRM Operations project execution systems
• Developing, vet and align on CRM campaign feasibility technical requirements and BRD
• Participating in all cross functional CRM project status meetings, leading the CRM channel tactics agenda and next steps.
• Managing relationships with internal cross-functional colleagues and external agencies to leverage their expertise and ensure successful execution of CRM initiatives
• Acting as a key enabler in building a strong culture and driving the Chief Marketing Office’s disruptive innovation agenda
• Staying informed about industry trends and emerging CRM technologies, proactively identifying opportunities for innovation and growth

Senior Manager, US CRM

• Architect and lead a best-in-class secondary analytics organization for the Specialty Care portfolio, setting the analytical agenda and translating brand strategy into rigorous analyses and measurement frameworks
• Build, develop, lead and retain a high-performing team of analysts; create a culture of intellectual curiosity, analytical rigor, and commercial impact
• Serve as a strategic thought partner to cross-functional partners, BU leaders and heads of Specialty Care overall/IIS, delivering insights that are clear, defensible, and decision-ready
• Drive deep patient and HCP insights using syndicated, claims, and novel data sources — moving beyond trend reporting to uncover the "why" behind commercial performance
• Frame, structure, and answer the hardest commercial questions facing Specialty Care leadership, including competitive dynamics, market evolution, launch performance, and long-range planning
• Partner across GCA — including Data Science, Forecasting, and Digital Analytics — to pioneer new analytical methods, integrate emerging data assets, and push the boundaries of what secondary analytics can do
• Establish and enforce standards for analytical quality, data governance, and insight communication across the Oncology analytics ecosystem