Medical Director

• Define and execute the development strategy of oncology program(s)
• Lead one or more subteams in clinical development
• Serve as the clinical lead across multiple clinical trials
• Provide oversight and management responsibilities of medical directors
• Accountable for clinical development strategy, trial design, execution, and results delivery
• Oversee the development and management of clinical protocols and amendments
• Lead peer-to-peer interactions with investigators
• Collaborate with Clinical Scientist to review and interpret clinical data.

Clinical Development Executive, Medical Director – GI Oncology

• Drive Quality Medicine & Patient Safety
• Ensure consistent delivery of high-quality, evidence-based care across hospitals
• Coach and develop Medical Directors through record reviews, hospital visits, and real-time feedback
• Champion patient safety initiatives, including event reporting and continuous improvement efforts
• Support adoption of new medical advancements, standards of care, and clinical best practices
• Partner with teams to improve client communication, case management, and follow-up care
• Oversee medical record quality, equipment standards, and clinical compliance
• Manage medical-related client concerns and board complaints through resolution
• Foster a culture of collaboration, accountability, and psychological safety
• Partner with Field Leadership, Medical Affairs, and operations to align priorities and execution
• Support recruiting, hiring, and onboarding of veterinarians, including new graduates
• Proactively identify and address medical, staffing, and operational challenges
• Serve as the medical voice within the field leadership team
• Mentor and grow Medical Directors and veterinarians through coaching and development planning
• Support onboarding, training, and integration of new doctors
• Guide teams on improving efficiency, productivity, and team-based care delivery
• Create an environment that supports continuous learning and career growth

Group Medical Director – Specialty

• Provide strategic leadership and clinical oversight for DSNP/FIDE complex populations.
• Lead a team of Senior Medical Directors/Medical Directors within the Center of Excellence (COE) Duals.
• Drive medical management programs and policies that improve quality, cost, and outcomes across the continuum of care.
• Ensure compliance, operational excellence, and superior member experience.
• Actively participate in scheduled team and leadership meetings supporting the EMD.

Lead Senior Medical Director, DSNP

• Responsible for medical and scientific oversight of clinical trials in Internal Medicine
• Provides timely, study-related medical information and guidance
• Conducts and documents periodic safety data review and ongoing clinical/medical data review
• Represents the study team in internal protocol review governance submissions and interactions
• Develops site selection criteria and ensures protocol training is delivered to site-facing colleagues
• Ensures TMF compliance for clinical documents
• Develops clinical guidance and reviews safety data

Clinical Development Medical Director, MD Required

• Serve as Clinical Trial Director for Phase 1–4 trials, designing study protocols and supplementary documentation, including study procedures manuals, analysis plans, and protocol deviation plans.
• Provide medical governance, ensuring clinical and operational excellence in study execution.
• Manage study conduct, enrollment strategies, and interpretation of clinical data.
• Provide expertise in managing safety events and toxicity concerns.
• Train internal and external teams on protocol-defined safety parameters.
• Ensure comprehensive documentation of trial-related inquiries and safety events in the electronic Trial Master File.
• Partner with internal teams in virology, pharmacology, biostatistics, drug safety, regulatory affairs, and discovery science to design efficient clinical studies.
• Collaborate with external investigators, consultants, institutional review boards (IRBs)/research ethics committees (RECs), and community stakeholders for trial feasibility, conduct, and reporting.
• Assist in developing submissions for regulatory bodies (U.S. and international) during and post-study phases.
• Prepare responses to regulatory queries and present clinical trial findings to internal governance groups.
• Foster strong professional relationships and teamwork within a matrix environment to drive project success.
• Thrive in a fast-paced, dynamic setting while demonstrating leadership and adaptability.
• Contribute to organizational growth and innovation, supporting the mission of global impact.

Medical Director, R&D Physician Center of Excellence

• 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 in order to contribute to Medical 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 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 Therapeutic Area
• 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
• Lead advisory boards (develop BRF, Agency collaboration) with manager oversight
• 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
• 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
• Provide 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

Field Medical Director – Oncology

• Develop and manage the Clinical Policy, Regulatory, and Compliance functions within the Office of Clinical Affairs.
• Ensure clinical operations meet healthcare laws and standards.
• Develop and maintain regulatory policies.
• Manage compliance risks and guide policy-related submissions.
• Advise senior leadership and work closely with teams across the organization.

Medical Director, Clinical Regulatory Affairs

• Work with Cross-functional teams to develop robust territory plans that impact and inform HCPs leading to improved patient outcomes
• Establish and maintain scientifically credible peer-to-peer scientific relationships with national & regional opinion leaders in addition to other healthcare providers
• Facilitate & monitor strategic partnerships with scientific/clinical experts and serve as an enterprise-level point of contact with organizations
• Support major and regional congresses by engaging thought leaders
• Provide balanced, accurate information to regional formulary decision makers and/or P&T committee members
• Identify and vet investigators, nominate sites to Clinical Operations for company-sponsored clinical trials as requested
• Assist in the development and execution of clinically relevant regional medical meetings

Field Medical Director – Solid Tumor, Breast and Lung

• providing clinical expertise to promote the delivery of high quality, constituent focused medical care with a focus on clinical and payment policy
• transactional reviews in support of the appeal process
• clinical claim review process
• predetermination of covered benefits in the Commercial and Medicare environments
• participate on work groups as a clinical subject matter expert to identify and promote opportunities to improve quality and efficiency of health care services
• apply clinical coding and reimbursement expertise to ensure alignment and correct application of Aetna policies and practices to service and payment requests
• proactively use data analysis to identify opportunities for quality improvement

Medical Director – Medical Policy Ops, DRG

• providing clinical expertise to promote the delivery of high quality, constituent focused medical care with a focus on clinical and payment policy
• transactional reviews in support of the appeal process, clinical claim review process, and predetermination of covered benefits in the Medicare and commercial environments, with emphasis on Medicare clinical and payment policy
• participate on work groups as a clinical subject matter expert to identify and promote opportunities to improve the quality and efficiency of health care services
• apply clinical, coding and reimbursement expertise to ensure alignment and correct application of Aetna policies and practices to service and payment requests
• proactively use data analysis to identify opportunities for quality improvement and positively influence the effective delivery of quality care services
• be a subject matter expert, internal consultant and payment policy contributor
• work collaboratively with the functional areas

Medical Director – Medical Policy & Operations

• Serve as the clinical authority for clinical data definitions and decision logic frameworks
• Build team capability in clinical data science and outcomes measurement
• Serve as the clinical informatics subject matter expert for product teams
• Review and approve clinical-facing content and logic for accuracy
• Partner with Data/Analytics and Data Science teams to define analytical approaches

Senior Medical Director – Clinical Informatics

• Provides medical monitoring on one or more clinical trials
• Provides timely, study-related medical information and guidance
• Conducts and documents periodic safety data review and ongoing clinical/medical data review
• Reviews required safety text for the Informed Consent Document
• May independently lead clinical execution of one or more studies
• Represents the study team in internal protocol review governance submissions
• Ensures development of Study Informed Consent Documents
• Develops site selection criteria and provides clinical input to selection of sites

• 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

• Provides strategic direction, professional oversight, and leadership throughout the precert process and other clinical operations.
• Collaborates with executive leadership to develop and implement strategies that align with healthcare objectives, improve processes, drive innovation, and positively impact members and providers.
• Leverages medical and operational expertise to develop and align the company's goals with clinical strategies and regulatory requirements.
• Collaborates with cross-functional leaders to shape and drive the clinical operations strategy and initiatives, ensuring optimal quality and efficiency.
• Establishes clinical standards and oversees clinical governance structures to ensure patient safety and the provision of quality care.
• Leads the development of clinical processes and programs, such as clinical protocols, guidelines, treatment pathways, and training curricula.
• Manages operations of the Medicare Precertification MD Team, in alignment with governing policies and procedures.
• Leads teams through Medicare audits and on-going audit readiness.
• Stays updated on relevant scientific evidence, industry standards, and regulatory changes to ensure organizational compliance and relevance.
• Develops and maintains relationships with key stakeholders, such as government agencies, providers, and professional organizations.
• Develops and continuously monitors key metrics to assess the performance of strategic initiatives and processes, making adjustments as needed.
• Provides mentorship, professional development opportunities, and support to physicians, promoting their growth and ensuring a cohesive and skilled medical team.
• Collaborates with legal and compliance teams to ensure developed clinical processes and solutions comply with all applicable regulatory requirements.

Senior Medical Director – Precertification

• 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

• Responsible for supporting clinical trial(s) and lead subteams in clinical development
• Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring
• Lead peer-to-peer interactions with investigator
• Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities
• Lead and contribute to development and maintenance of clinical trial and regulatory documents
• Oversees and provides clinical development leadership across several study teams
• Collaborates with the Global Development Team to create and refine development strategies
• Represents the company in external engagements or in committee members

Senior Medical Director, Clinical Development – Breast Oncology

• 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

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Clinical Development Executive, Medical Director – GI Oncology

Group Medical Director – Specialty

Lead Senior Medical Director, DSNP

Clinical Development Medical Director, MD Required

Medical Director, R&D Physician Center of Excellence

Field Medical Director – Oncology

Medical Director, Clinical Regulatory Affairs

Field Medical Director – Solid Tumor, Breast and Lung

Medical Director – Medical Policy Ops, DRG

Medical Director – Medical Policy & Operations

Senior Medical Director – Clinical Informatics

Clinical Development Medical Director, MD Required

Field Medical Director – Breast and Gynecologic Cancers

Senior Medical Director – Precertification

Clinical Development Medical Director, Hematology

Senior Medical Director, Clinical Development – Breast Oncology

Clinical Development Medical Director, Oncology