Senior Medical Director, Clinical Development – Oncology

• Provide clinical development expertise for late-stage thoracic oncology clinical trials
• Oversee clinical trial design, conduct, and analysis
• Supervise other associate medical directors as needed
• Collaborate with regulatory affairs, pharmacovigilance, biostatistics, medical affairs, clinical operations, investigators, health authorities, ethics committees, and patient advocacy groups
• Conduct medical monitoring, including eligibility assessment, data review, and safety monitoring
• Lead peer-to-peer interactions with investigators
• Serve as point of contact for clinical issues among study teams, investigators, ethics committees, steering committees, and regulatory authorities
• Lead and contribute to clinical trial and regulatory documents
• Participate in the Clinical Subteam of the Global Product Team to execute clinical development strategies
• Represent Pfizer in advisory boards and health authority interactions
• Review and interpret clinical data, identify key findings and implications, and communicate them to stakeholders
• Maintain current clinical expertise by following developments, literature, and guidelines
• Report to the Clinical Development Executive Medical Director and partner with cross-functional subject-matter experts and counterparts in other Pfizer divisions
• Influence and collaborate with peers, develop and coach others, and oversee colleagues' work to achieve outcomes and business impact

• Medical degree required
• 5+ years of industry experience required
• Clinical Development experience required
• Primary medical degree (e.g., MD, DO, MBBS, MBChB) from a recognized medical school or university
• Licensed by a licensing body or health authority to prescribe medicines independently of supervision for at least 2 years after the intern/house officer/foundation period
• Late-stage clinical development experience preferred
• Thoracic Oncology experience preferred
• Board certified or eligible in oncology, or equivalent, preferred
• Maintained registration or medical license to practice and always been in good standing with the Medical Licensing Authority, preferred
• Must be authorized to be employed in the U.S. by any employer
• Permanent work authorization in the United States required
• U.S. work visa sponsorship is not available now or in the future
• Travel to scientific conferences or meetings several times per year, as needed

Demonstrates expertise in clinical development for late-stage thoracic oncology trials, with a strong focus on trial design, medical monitoring, and regulatory collaboration. Possesses a medical degree and extensive experience in clinical development, ensuring compliance and effective communication with stakeholders.

• Clinical Development Expertise
• Medical Monitoring
• Regulatory Collaboration
• Thoracic Oncology Experience
• Medical Degree

• Clinical Trial Design
• Data Review
• Safety Monitoring
• Eligibility Assessment
• Clinical Data Interpretation
• Regulatory Document Contribution
• Clinical Development Strategy Execution
• Peer-to-Peer Interactions
• Advisory Board Representation
• Cross-Functional Collaboration

• Leadership
• Coaching
• Influencing
• Collaboration
• Communication

• Board Certification in Oncology
• Medical License

• Thoracic Oncology
• Clinical Trials
• Pharmacovigilance
• Biostatistics
• Health Authorities
• Ethics Committees
• Patient Advocacy
• Clinical Operations
• Global Product Team
• Scientific Conferences