Pfizer

Medical Director

• Provides medical monitoring on one or more clinical trials
• Provides timely, study-related medical information and guidance
• Contributes to medical assessments of Quality Events
• Conducts and documents periodic safety data review and ongoing clinical/medical data review
• Reviews Required Safety Text for the Informed Consent Document
• Provides clinical support for one or more studies
• May provide input to the protocol design document
• Supports the study team in internal protocol review governance submissions and interactions
• May develop Study Informed Consent Documents
• Provides clinical input to the development of the Statistical Analysis Plan
• Ensures all clinical queries are appropriately addressed in support of database lock
• Tracks and reconciles Serious Adverse Events
• Contributes to site selection criteria
• May serve as a clinical point of contact with investigators and study team for questions relating to clinical aspects of the protocol

Clinical Development Medical Director – Associate Director

Compliance

• Your role will involve interpreting federal, state, and international regulations as they apply to our products, processes, practices, and procedures.
• You will investigate and resolve compliance issues both within and outside of Pfizer, ensuring that our commitment to excellence and integrity remains steadfast.
• The Quality Oversight and Compliance Director is responsible for developing and maintaining Quality Plans, ensuring inspection and audit readiness, providing quality oversight of process deviations, investigations and associated corrective and preventive actions, and driving compliance of pan-regulatory (e.g. Manufacturing, Regulatory Strategy, CMC, Submissions, Clinical) information and processes globally.
• The Quality Oversight and Compliance Director works to instil a quality mindset by ensuring the quality and compliance of regulatory processes and product/license information through clearly defined and documented metrics, identifying data trends and addressing associated process risks in collaboration with Regulatory Process Business Process Owners (BPOs) and stakeholders.
• The Quality Oversight and Compliance Director works with Regulatory Process BPOs and stakeholders to identify and investigate procedural/compliance gaps and deviations, identify root cause and establish/monitor appropriate remediation plans through timely completion.
• The Quality Oversight and Compliance Director supports and drives implementation of inspection readiness, audit preparedness and training compliance.
• Develop and lead/co-lead highly complex projects, creating mid-term plans that impact results and drive innovation.
• Identify critical quality process parameters/KPIs to ensure data and process quality and collaborate to create associated Quality Plans and metric reports/dashboards.
• Provide oversight of existing and input to planned processes/ systems /controls to ensure that quality is built-in to enable consistent compliance.
• Identify procedural/compliance gaps associated with in scope processes and establishes mitigation and remediation plans with BPOs that provide optimal balance of compliance and business need.
• Drive the investigation, remediation and closeout of Quality Events and associated corrective and preventive actions.
• Drive and support inspection readiness activities and provide remediation support for audit (or inspection) findings.
• Identify opportunities for improvement of pan-regulatory data and business processes and procedures through the definition, management and analysis of metric data in collaboration with BPOs and other stakeholders.
• Leverage relationships to meet the needs of various business units, serving as an advisor and influencing management decisions.
• Make decisions in complex problems, recommend innovative solutions, and support in solving issues impacting business units.
• Act independently on self-initiated projects, using knowledge and judgment in complex decisions within business units.
• Guide Pfizer by interpreting regulations and designing compliance programs, conducting audits, and evaluating policies.
• Provide expertise on quality standards, support partner functions globally, and drive risk management and quality oversight.

Quality Oversight and Compliance Director

Software Engineer

• Lead or co-lead moderate to complex projects, effectively managing time and resources.
• Apply skills and discipline knowledge to contribute to departmental work.
• Resolve moderately complex problems and develop new options in non-standard situations, operating independently in ambiguous contexts.
• Work independently on assignments, receiving guidance on unusual or complex issues.
• Review your own work and seek directional feedback, potentially mentoring other colleagues.
• Utilize judgment and experience, potentially serving as a resource for others.
• Coordinate and manage manufacturing technical processes and functions to support technical projects.
• Identify and implement cost-saving ideas, focusing on efficiency and equipment capacity improvements.
• Ensure all projects comply with Current Good Manufacturing Practices, regulatory standards, and safety requirements.
• Develop objectives for assignments and operate independently, especially in ambiguous situations.

Manager, Process Engineering – Sterile Inspection

• Plan and execute medical strategy and engagement for assigned customers
• Maintain knowledge of relevant TA/disease states and Pfizer medicines
• Serve as a resource for medical information and customer insights
• Understand priorities of Pfizer Medical Affairs
• Maintain effective communication among medical colleagues
• Deliver approved medical content about Pfizer medicines
• Identify and seek medical engagement from priority customer segments
• Provide truthful, accurate, and scientifically supported information to HCPs
• Facilitate medical support throughout Investigator Sponsored Research (ISR) process
• Cultivate research and TA expertise
• Represent Pfizer Medical Affairs leadership

Oncology Field Medical Director – MD

Manager

• Provide therapeutic area/product expertise in genitourinary oncology across medical customer segments
• Plan and execute medical strategy for assigned customers
• Maintain required knowledge of relevant TA/disease states and Pfizer medicines
• Serve as a resource for medical information and customer insights
• Understand priorities of Pfizer Medical Affairs to contribute to medical content strategy
• Maintain effective communication among medical colleagues and other Pfizer staff
• Optimize patient centricity in medical communications
• Deliver approved medical content about Pfizer medicines
• Identify and seek medical engagement from priority customer segments
• Provide accurate information in response to medical requests from HCPs
• Partner with Global Medical Affairs and identify potential sites for clinical trials
• Cultivate research and TA expertise

Senior Oncology Field Medical Manager

Director

• Shape how Oncology businesses enable its field force
• Lead enterprise-level reporting, analytics, and CRM programs
• Serve as a strategic thought partner in Oncology Customer Engagement & Performance Leadership
• Enable effective deployment of new capabilities across Commercial Enablement Excellence
• Identify and scale internal and external best practices for field force effectiveness
• Provide strategic guidance on CRM core design and reporting strategy
• Own enterprise HCP Access capability and assess impact of capabilities

Senior Director, CFC Enablement Lead – Oncology

• Plan and execute medical strategy and engagement with appropriately identified customers within an assigned territory
• Maintain a high level of scientific and therapeutic area knowledge, including disease states, standards of care, emerging data, and Pfizer medicines
• Deliver truthful, balanced, accurate, and scientifically supported information in response to unsolicited medical requests from HCPs
• Serve as a conduit for medical information and customer insights
• Identify and explore areas where real‑world clinical practice may diverge from established evidence
• Maintain effective communication and collaboration with headquarters Medical Affairs colleagues
• Demonstrate strong communication skills across multiple channels
• Optimize patient centricity in medical communications and engagements
• Support patient‑focused discussions that highlight unmet needs across care settings
• Deliver approved medical content related to Pfizer medicines to HCPs across a variety of settings
• Identify, prioritize, and engage appropriate customer segments within the assigned therapeutic area
• Field and manage inbound medical inquiries through established Pfizer triage processes
• Partner with Global Medical Affairs and Worldwide Research & Development for Pfizer‑sponsored clinical trials
• Provide medical support throughout the Investigator Sponsored Research (ISR) lifecycle
• Cultivate research and therapeutic area expertise
• Reactively and proactively engage with local patient advocacy organizations
• Deliver insights regarding local patient organization structures
• Serve on therapeutic area, asset, and cross‑functional committees or initiatives

Senior Manager, Field Medical, non-MD

• Plan and execute medical strategy and engagement with identified customers
• Maintain a high level of scientific and therapeutic area knowledge
• Deliver accurate and scientifically supported information in response to medical requests from HCPs
• Serve as a conduit for medical information and customer insights
• Identify gaps between evidence-based standards of care and clinical practice
• Maintain effective communication and collaboration with internal colleagues
• Optimize patient centricity in medical communications
• Deliver approved medical content related to Pfizer medicines to HCPs
• Partner with Global Medical Affairs to support clinical trials

Senior Manager, Field Medical

• Partner with internal customers to identify and evaluate available sourcing and resourcing options
• Prepare a Request for Information and investigate alternative vendor solutions
• Independently prepare commercial terms & conditions and execute medium complexity contracts
• Liaise frequently with stakeholders to manage expectations of sourcing and contracting process
• Directly negotiate changes to standard contract language
• Participate in special projects and/or initiatives to achieve business objectives

Manager – Flexible Resource Strategy

• Be a field-based medical colleague on the Payer Team responsible for providing therapeutic area/product expertise within Oncology
• Educate customers on the clinical and economic impact of Pfizer Oncology medicines
• Help inform customer decision-making and improve population health through real-world data analyses
• Contribute to Pfizer’s ability to plan and execute Oncology Medical strategy
• Maintain effective communication and collaboration among headquarters Medical colleagues
• Demonstrate expertise in communication across multiple channels
• Integrate clinical, Health Information Technology (HIT), market, and account considerations to develop customer-specific projects
• Facilitate communication between regional and national HCPs and headquarters Medical Affairs colleagues
• Maintain a status for internal training requirements

Oncology Outcomes Director, Non-MD

• Provide therapeutic area/product expertise across a broad range of medical customer segments
• Plan and execute Medical strategy and engagement for assigned customers within a territory
• Maintain knowledge of relevant TA/disease states and Pfizer medicines
• Serve as a conduit for Medical Information and customer insights
• Understand Pfizer Medical Affairs priorities to contribute to Medical content strategy development
• Maintain effective communication among Medical colleagues
• Demonstrate expertise in communication across multiple channels
• Optimize patient centricity of Medical communications and deliverables
• Deliver approved medical content about Pfizer medicines
• Identify and seek medical engagement from priority customer segments
• Provide scientifically supported information in response to requests from HCPs
• Collaborate with Global Medical Affairs colleagues for clinical trial site identification
• Provide Medical support throughout the Investigator Sponsored Research (ISR) process
• Cultivate research and therapeutic area expertise

Oncology Field Medical Director – Thoracic, Non-MD

• Plan and execute Medical strategy and engagement for appropriate 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
• Understand the priorities of Pfizer Medical Affairs in order to contribute to Medical content strategy development
• Maintain effective and appropriate communication and collaboration among headquarters Medical colleagues
• Demonstrate expertise in communication across multiple channels
• Optimize patient centricity of Medical communications and deliverables
• Deliver approved medical content about Pfizer medicines and relevant topics
• Identify and seek medical engagement from priority customer segments in assigned Therapeutic Area
• Provide truthful, accurate, and scientifically supported information in response to direct unsolicited medical requests
• Collaborate with Global Medical Affairs colleagues
• Provide Medical support throughout the Investigator Sponsored Research (ISR) process
• Cultivate research and therapeutic area expertise
• Provide Asset leadership
• Reactively and proactively communicate with local Patient Advocacy Group(s) as appropriate
• 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
• Participate in special projects as needed

Oncology Field Medical Director – Thoracic

Vice President

• Set the US brand vision and mobilize a cross-functional operating model.
• Lead end-to-end US strategy from pre-launch through launch and into sustained performance.
• Own investment governance and outcomes, partnering closely with Finance and senior franchise leadership.
• Provide executive leadership for development of best-in-class HCP and patient strategy.
• Identify, prioritize, and resource growth opportunities.
• Establish performance management and analytics governance for US marketing initiatives.
• Lead brand financial stewardship including Annual Operating Plan.

Vice President, US Brand Lead – Sigvotatug Vedotin

• Deliver approved medical content about Pfizer medicines and relevant topics
• Identify and seek medical engagement from priority customer segments
• Provide truthful, accurate, and scientifically supported information in response to direct unsolicited medical requests from HCPs
• Lead advisory boards with manager oversight
• Field relevant inbound queries from HCPs via established triage process
• Collaborate with Global Medical Affairs colleagues
• Cultivate research and therapeutic area expertise
• Provide Asset leadership
• Reactively and proactively communicate with local Patient Advocacy Group(s)
• Serve on Medical and/or TA and asset cross-functional committees
• Represent Pfizer Medical Affairs leadership with clinical/professional associations
• Mentorship and onboarding partner
• Participate in special projects as needed

Field Medical Director – Breast and Gynecologic Cancers

• Provide therapeutic area/product expertise for the designated therapeutic area across a broad range of Medical customer segments and initiatives in an assigned territory (MA, CT, NH, VT, RI, ME, Upstate NY).
• Plan and execute Medical strategy and engagement for appropriate 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.
• Understand the priorities of Pfizer Medical Affairs to contribute to Medical content strategy development and execute aligned Field Medical tactics.
• Demonstrate expertise in communication across multiple channels.
• Optimize patient centricity of Medical communications and deliverables.