Senior Manager, Oncology Late Stage Clinical Development
Pfizer
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Posted: 10/20/2026Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical trial oversight and regulatory compliance, with a strong focus on oncology development strategies and data integrity. Proficient in authoring clinical documents and collaborating with cross-functional teams to optimize clinical procedures and ensure successful regulatory submissions.
Highest-signal resume keywords
PhD/Pharm D In Relevant Science DisciplineClinical Research Experience In OncologyKnowledge Of ICH Guidelines And GCPExperience With Regulatory SubmissionsProficiency In Microsoft Office And Scientific Software
Tech Stack
Tools & technologiesAbout the role
Key responsibilities & impact- Provide scientific oversight, data integrity and quality oversight for clinical trials supporting late-stage oncology development strategies
- Serve as clinical development expert for assigned studies and maintain current scientific and clinical knowledge in the relevant therapeutic and disease areas
- Partner with clinical and medical colleagues, clinical operations and other functional teams to implement and execute clinical trials
- Represent study teams in governance meetings and submissions; support Development Leads and Medical Directors on study and disease-area strategy
- Author protocols and study-level informed consent documents
- Contribute to investigator brochures, site training materials, clinical study reports, regulatory responses and other clinical and regulatory documents
- Support preparations for Health Authority meetings and participate as appropriate
- Set clinical data review strategies; lead collection and review of quality and emerging clinical data and trends
- Review and query data and present relevant data to teams, governance bodies and internal and external stakeholders
- Analyze the emerging safety profile of drugs with medically qualified colleagues and communicate changes to clinical and safety colleagues
- Follow SOPs and regulations, complete applicable training and improve the quality and efficiency of clinical procedures
- Lead or participate in portfolio- and enterprise-level workgroups optimizing clinical development procedures
- Serve as a subject matter expert or business process owner for relevant SOPs or procedures
Requirements
What you’ll need- PhD/Pharm D in a relevant Science discipline and minimum of 2 years Clinical Research experience in industry/CRO, OR MS in a relevant Science discipline and minimum of 5 years of Clinical Research experience in industry/CRO, OR BA/BS in a relevant Science discipline and minimum of 7 years Clinical Research experience in a similar role in industry/CRO
- Experience in oncology clinical trial development, solid tumor and/or heme
- Clinical Research experience in the phase 3/pivotal space in Oncology, ideally on the side of the sponsor and 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
- Extensive understanding of Clinical Operations, Safety, Biostatistics, Regulatory, Study Management, Pre-clinical, Pharmacology, and Quality Assurance
- Experience working on large data sets
- Proficiency with Microsoft Office and relevant scientific software
- Effective communication, presentation, and organizational skills
- Experience leveraging a variety of communication tools and techniques to communicate results
- Experience solving problems collaboratively and handling conflict constructively
- Track record of scientific productivity evidenced by publications, posters, abstracts and/or presentations
- Experience working proactively and independently, organizing tasks, time and priorities of self and others
- Experience building partnerships across the company
- Candidates must be authorized to be employed in the U.S. by any employer
- U.S. work visa sponsorship is not available for this role now or in the future
- Requires permanent work authorization in the United States
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
- Medical, prescription drug, dental and vision coverage
- Bonus target of 17.5% of base salary through Pfizer’s Global Performance Plan
- Eligibility to participate in Pfizer’s share based long term incentive program
- Relocation assistance may be available based on business needs and/or eligibility
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial DevelopmentData Integrity OversightRegulatory ComplianceClinical Procedures KnowledgeBiostatistics UnderstandingQuality AssuranceSolid Tumor ExperiencePhase 3 Clinical ResearchSafety Profile AnalysisLarge Data Set Management
Soft Skills
Effective CommunicationPresentation SkillsOrganizational SkillsCollaborative Problem SolvingConflict Resolution
Industry Keywords
OncologyClinical OperationsFDA RegulationsEMA RegulationsSOPsClinical Development ProceduresHealth Authority MeetingsInvestigator BrochuresClinical Study ReportsScientific Productivity