Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Pfizer

Senior Medical Director, Clinical Development – Oncology

Pfizer

Senior Medical Director guiding Pfizer's late-stage thoracic oncology clinical development. Overseeing trial design, conduct, analysis, medical monitoring, and cross-functional regulatory collaboration.

Posted 8/17/2026full-timeNew York City • California, Connecticut, Massachusetts, New York, Washington • 🇺🇸 United StatesSenior💰 $274,500 - $457,500 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

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.

Highest-signal resume keywords
Clinical Development ExpertiseMedical MonitoringRegulatory CollaborationThoracic Oncology ExperienceMedical Degree

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial DesignData ReviewSafety MonitoringEligibility AssessmentClinical Data InterpretationRegulatory Document ContributionClinical Development Strategy ExecutionPeer-to-Peer InteractionsAdvisory Board RepresentationCross-Functional Collaboration
Soft Skills
LeadershipCoachingInfluencingCollaborationCommunication
Certifications & Qualifications
Board Certification in OncologyMedical License
Industry Keywords
Thoracic OncologyClinical TrialsPharmacovigilanceBiostatisticsHealth AuthoritiesEthics CommitteesPatient AdvocacyClinical OperationsGlobal Product TeamScientific Conferences

About the role

Key responsibilities & impact
  • 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

Requirements

What you’ll need
  • 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

Benefits

Comp & perks
  • Pfizer Global Performance Plan with a bonus target of 25.0% of the base salary
  • Share based long term incentive program
  • 401(k) plan with Pfizer Matching Contributions
  • Additional Pfizer Retirement Savings Contribution
  • Paid vacation
  • Paid holidays
  • Paid personal days
  • Paid caregiver/parental leave
  • Paid medical leave
  • Medical coverage
  • Prescription drug coverage
  • Dental coverage
  • Vision coverage
  • Relocation assistance may be provided
  • Relocation assistance may be available based on business needs and/or eligibility