Pfizer

Compliance

• Lead, develop and support execution of PharmSci Audit strategic plan
• Work in partnership with RQA on the internal audit plan
• Analyze data to support audit and inspection management, regulatory compliance, and strategic planning
• Ensure that the audit, inspection management and regulatory surveillance quality systems are a competitive advantage for PharmSci
• Collaborate across the PharmSci network to standardize practices
• Implement strategies for performance improvement and deploy metrics to determine effectiveness
• Partner with PharmSci Business Lines, RQA and PGS to develop procedures and plans for audits, inspections and regulatory information management
• Support the management of audit, inspection and regulatory information systems for PharmSci
• Function as a Quality System Subject Matter Expert

PSOQ Audit, Inspection Management, Regulatory Surveillance Strategic Process Lead

Marketing

• NVAF Marketing lead -- optimize core NVAF promotion
• Lead Retail HCP Promotional Campaign strategy and development
• Identify, commercialize new NVAF data and relevant guidelines
• Build and evolve retail and NVAF strategy through advanced analytics, research, targeting
• Lead patient subpopulation evaluation & opportunity assessment
• Improve NVAF Rx adherence
• Inform NVAF specific content development for POA
• Identify and recommend novel ways to increase awareness of DOAC benefits in underserved communities via HCPs
• Serve as POC for retail CV Field Force
• Serve as CV STEM executional optimization brand lead
• Evolve HCP commercial strategy short term and in peri-LOE phase
• Optimize and innovate field force digital sales tools via the E-Source digital sales presentation platform
• Pull through NVAF market expansion strategies to the field force
• Serve as Dynamic Targeting and Dynamic Content (AI initiatives) brand lead

Director, HCP Marketing

Manager

• Provide strategic input into clinical trial designs (eg, patient populations, comparators, endpoints) and analysis plans to enable successful negotiations, reimbursement, and appropriate patient access with global payer and regulatory decision makers.
• Develop and execute the clinical outcomes assessment strategy and incorporate humanistic and economic endpoints into clinical trials across all phases of product development to build comprehensive trial-based evidence aligned with overall asset strategy and to ensure global reimbursement and access requirements.
• Help to develop and execute the Value & Evidence Strategy (VES) to support the value of this innovative therapy in close partnership with the cross-functional matrix team and local country/regional teams.
• Lead the design and execution of global HEOR studies (eg, network meta-analyses, non-interventional studies, economic models) from concept through publication.
• Lead the timely development of reimbursement deliverables to successfully support reimbursement and access requirements in conjunction with the regions/countries.
• Partner with internal stakeholders to ensure appropriate customer-facing dissemination of HEOR materials.
• Develop strategic partnerships and research collaborations with key external experts, healthcare policy makers, payers, and various academic and community oncology settings to support asset strategies.
• Remain fully compliant with all Pfizer SOPs (standard operating procedures).

Senior Manager, HTA, Value and Evidence – Solid Tumors

Program Manager

• Provide comprehensive support to Pfizer Oncology’s Global Regulatory Strategy Teams (GRST) and Submission Teams
• Develop and manage submission timelines and milestones using appropriate tools
• Identify efficiencies to enable fast filings and convert submission timelines into clear, actionable tasks with proactive follow-up to ensure on-time delivery
• Contribute to the design and implementation of processes that enhance workflow efficiency and provide guidance on best practices and procedures
• Organize and manage GRST, Submission Team, MCI and other leadership pre-alignment meetings
• Proactively identify and resolve project issues to meet productivity, quality, and organizational goals
• Lead or co-lead projects, effectively managing time and resources for oneself, with consideration of impact on team members
• Develop and maintain templates, dashboards, team rosters, document reviewer lists, SharePoint/Teams sites, and action trackers
• Independently prepare comprehensive status reports, timelines, tables, graphs, correspondence, and presentations as needed for internal and external stakeholders
• Track and analyze metrics to support business insights
• Assist with onboarding of new team members and provide training and guidance for new project system users

Manager, Regulatory Program Management – Submission Strategy, Oncology

General Counsel

• Advise and counsel PGS BD, External Supply, PC1, PGS Procurement, and the Global Supply Chain teams on negotiation, drafting, and alliance management for supply–related transactions
• Support Quality organization on quality issues that may impact supply of product and related work with External Supply and PC1 on transactional matters
• Serve as a manufacturing and supply subject matter expert for other Pfizer Legal Division practice groups
• Participate in template and training teams to develop appropriate documents for supported client groups and drive efficient use of the templates for routine agreements by the clients, with support from legal professionals as appropriate

Corporate Counsel, Global Supply

Director

• Drive development and execution of the global value and evidence generation strategy
• Support and coordinate evidence needs input from global and country teams
• Lead the review and interpretation of clinical trial outputs
• Contribute to the design, execution, and oversight of HV&E studies
• Develop and maintain global value narratives and evidence deliverables
• Engage with cross-functional teams to position evidence strategy for rapid access upon launch
• Collaborate closely with alliance partners on evidence strategy

Director, HTA, Value & Evidence – HV&E, I&I / Brepocitinib

Software Engineer

• Conduct original research in computational protein engineering, with an emphasis on sequence- and structure-based generative modeling for protein fiducial design
• Develop and deploy state-of-the-art ML methods for multi-objective, constraint-aware protein optimization
• Apply proprietary computational framework and ML models for protein developability engineering
• Communicate research findings through manuscripts, conference presentations, and internal seminars
• Be an active member of a highly interdisciplinary team, collaborate with computational and experimental researchers in a multidisciplinary research environment

Postdoctoral Fellow – Generative AI for Protein Engineering

• Assumer la responsabilité générale de l’élaboration et de la mise en œuvre de la stratégie d’étiquetage
• Gérer le processus complet d’étiquetage ciblé aux premiers stades de développement
• Rédiger du nouveau contenu d’étiquetage en se fondant sur des données sources scientifiques
• Gérer l’équipe de l’Étiquetage interfonctionnelle et collaborer avec les parties prenantes
• Gérer les négociations touchant le libellé des documents avec la FDA des États-Unis et l’EMA
• Agir en tant que représentant principal en matière d’étiquetage auprès des équipes Stratégies des affaires réglementaires

Chef – Global Labeling Lead, Manager

Affiliate Manager

• Обеспечение глубокого вовлечения в образовательный и научный контент.
• Обеспечение прямого доступа к экспертным знаниям специалистов здравоохранения
• Прямое взаимодействие со специалистами здравоохранения в медицинских учреждениях больниц и клиник по вопросам предоставления пациентам необходимой информации
• Прямая линия связи со специалистами здравоохранения в отношении предоставления информации для оптимального выбора лечения пациентов
• Активное участие в повышении осведомленности и формировании инициатив по обеспечению доступа пациентам
• Ориентация на предоставление образовательных и научных материалов, а также инициатив, направленных на улучшение результатов и/или повышение качества поддержки специалистов здравоохранения.
• Активность по продвижению препаратов компании
• Поддержка достижения улучшенных результатов лечения пациентов посредством обучения врачей и пациентов, и предоставления услуг на основе глубокой научной экспертизы.

Health Solution Partner

Chief Marketing Officer

• The PAVE (Portfolio Alternative Value Enablement) team is an exciting new Business Unit in the US Commercial organization.
• PAVE was formed to enable continued patient access by maximizing value in mature, alliance and royalty assets.
• PAVE accomplishes this goal by changing asset trajectories by using innovative, lean, AI-enabled go-to-market models that unlock potential.
• Our team operates with a bold, ambitious and financially focused portfolio mindset.
• We build capabilities with an entrepreneurial culture that emphasizes speed, collaboration, and disciplined execution to create a unique end-to-end commercial learning environment.
• This secondment focuses on Marketing Operations and Marketing for the largest portion of the PAVE portfolio – the 11 promoted Oncology and General Medicine brands, which generate >$1B in revenue.
• The Secondee will play a critical role in leading development of promotional content, both new and derived from prior materials, by collaborating with our third-party partner, Indegene.
• Equally important, the Director will actively guide operationalization, ensuring compliance through MLR review and GCMA approval.

Marketing Director – Secondment

Backend Engineer

• Der NM ist verantwortlich für die Umsatz-/Absatz-Zielerreichung definierter Produkte/Produktportfolio(s)
• Eigenständige Analyse der Kunden- und Accountdynamik und deren Bedürfnisse
• Aufbau und Ausbau von belastbaren Beziehungen zu Schlüsselkunden und/oder Accounts
• Identifizierung, Etablierung, Ausbau und Pflege von Kundennetzwerken
• Vernetzt Kunden und fokussiert sich auf den Ausbau und die Optimierung von sektor- und/oder fachübergreifenden Überweisungs- und/oder Behandlungsstrukturen
• Planung, Organisation und Durchführung von kundenrelevanten Projekten, Services und Veranstaltungen
• Tagesaktuelle Dokumentation der Kundeninteraktionen
• Verantwortung zur Förderung der Nutzung/Vernetzung von neuen digitalen Angeboten und Plattformen

Fachreferent Brustkrebs, Network Manager Onkologie

LLM Engineer

• Design, implement, and own large-scale cloud-based HPC and MLOps platforms
• Architect multi-environment clusters (AWS, GCP, Azure)
• Lead the development of developer and cloud platforms
• Design, implement, and manage unified platform catalogs
• Build and maintain Python-based automation frameworks
• Operationalize ML model serving at scale
• Mentor engineers and lead cross-functional teams for integrated solutions

Staff Engineer, AI Infrastructure – MLOps

Account Executive

• Promote and sell defined products by conveying scientific messages and content to achieve established sales targets
• Ensure continuous improvement of customer experiences across all available channels and touchpoints
• Plan and monitor the use of communication channels preferred by customers
• Independently analyze territory dynamics and customer needs
• Responsible for promoting customer adoption/engagement with new digital offerings and platforms
• Build, maintain and, where appropriate, optimize resilient relationships with customers
• Plan, organize and execute local projects, services and events

Sales Rep Specialist Gastroenterology I&I

• Responsible for the medical-scientific support of regional, national and international clinical and scientific experts
• Initiation, coordination and support of a wide range of medical education and research projects
• Close collaboration within a cross-functional team including Medical, Marketing and Sales
• Organize regional and national advisory boards in the field of breast cancer
• Support and evaluation of current clinical research results and key publications in the relevant oncology indications

Medical Affairs Scientist, Field Oncology – Breast Cancer Northeast

• Shape and enhance Pfizer’s US migraine congress strategy
• Lead planning and execution of 20+ annual society meetings
• Attend select key congresses to support booth, executive encounters, and other tactical execution
• Refine Pfizer’s society partnership strategy
• Support local exhibit and display tactics & logistics
• Collect insights and metrics to evaluate performance
• Work seamlessly across different functional teams
• Oversee other agency partners handling CFC and congress assets