Senior Director – Oncology Late Stage Data Review

Pfizer

. Responsible for setting the data oversight, integrity, analysis, quality, and consistent adoption of AI and best practices in support of the data strategy for the Late-Stage Oncology portfolio.

Posted 5/10/2026full-timeCambridge • California, Massachusetts, New York, Washington • 🇺🇸 United StatesSenior💰 $214,900 - $358,100 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Responsible for setting the data oversight, integrity, analysis, quality, and consistent adoption of AI and best practices in support of the data strategy for the Late-Stage Oncology portfolio.
Manage and/or mentor colleagues and/or contingent workers across several indications in Oncology, providing clarity of purpose and priorities.
Develop talent within the team.
Serve as Clinical development data and AI expert for assigned late stage (Phase 2-3) studies maintaining clinical knowledge in the specific therapeutic and disease area(s) of assignment.
Effectively partners with other clinical and medical colleagues, clinical operations, data management, digital, and other functional lines for the successful implementation and execution of the clinical data deliverables within the Oncology Late Stage Portfolio.
Set the clinical data review strategy and lead the team in the review, reporting, and optimization of the data analysis; present to stakeholders as needed.

Requirements

What you’ll need

Science related PhD or PharmD and minimum of 7 years of Clinical Research experience in a similar role in industry, OR MS degree and a minimum of 10 years of Clinical Research experience in industry, OR BA/BS and minimum of 12-year Clinical Research experience in a similar role in industry.
Clinical Research and data experience in the phase 3/pivotal space in Oncology on the side of the sponsor with a track record of successful regulatory submission, inspection, and regulatory approval.
Excellent knowledge of clinical procedures, ICH guidelines, GCP and familiarity with FDA, EMA, and global regulations.
Experience in application of AI in streamlining and accelerating data review activities, reporting, and visualization.
Experience working with large data sets.
Strong experience working with cross functional internal and externals stakeholders.
Strong communication skills (verbal, presentation as well as experience leveraging a variety of communication tools and techniques to communicate results.
Minimum of 10 years of supervisory experience with groups of 10 to 20 team members.

Benefits

Comp & perks

401(k) plan with Pfizer Matching Contributions
Additional Pfizer Retirement Savings Contribution
Paid vacation
Holiday and personal days
Paid caregiver/parental and medical leave
Health benefits including medical, prescription drug, dental, and vision coverage

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Clinical ResearchData AnalysisAI ApplicationData IntegrityData QualityData OversightRegulatory SubmissionData VisualizationLarge Data SetsClinical Procedures

Soft Skills

MentoringTeam DevelopmentCross-Functional CollaborationCommunicationLeadershipPresentation SkillsClarity of PurposeStakeholder EngagementOrganizational SkillsPrioritization

Certifications

PhDPharmDMS DegreeBA/BS