Oncology Late Stage Clinical Development Scientist – Director

Pfizer

. Provide scientific oversight, data integrity and quality oversight of clinical trials supporting Late-Stage Oncology portfolio development strategies .

Posted 11/5/2026full-timeUnited StatesLead💰 $176,600 - $294,300 per yearWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in Clinical Research with a focus on Late-Stage Oncology, including protocol authorship, regulatory submissions, and data integrity oversight. Proficient in leading clinical trials, collaborating across functions, and ensuring compliance with ICH guidelines and GCP standards.

Highest-signal resume keywords

PhD/Pharm D In Relevant Science DisciplineClinical Research Experience In OncologyRegulatory Submission And Approval ExperienceLeadership Experience In Clinical TrialsKnowledge Of ICH Guidelines And GCP

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 AnalysisProtocol DevelopmentRegulatory DocumentationClinical Data ReviewOncology Clinical ResearchSolid Tumor And Hematology ExperienceBiostatisticsQuality AssurancePharmacology

Soft Skills

Effective CommunicationOrganizational SkillsCollaborative Problem SolvingConflict ResolutionPresentation Skills

Tools & Technologies

Microsoft OfficeScientific Software

Industry Keywords

Clinical OperationsFDA RegulationsEMA RegulationsICH GuidelinesGCP ComplianceClinical Research Organization (CRO)Pivotal TrialsStudy ManagementEmerging Drug Safety ProfilesHealth Authority Meetings

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Provide scientific oversight, data integrity and quality oversight of clinical trials supporting Late-Stage Oncology portfolio development strategies
Serve as clinical development expert for assigned studies and maintain current scientific and clinical knowledge
Partner with clinical and medical colleagues, clinical operations and other functions to implement and execute clinical trials
Represent study teams in governance meetings and submissions
Support the Development Lead/Medical Director on study and disease-area strategy
Author protocols, study-level informed consent documents, investigator brochures, training materials, clinical study reports, regulatory responses and other clinical/regulatory documents
Support Health Authority meeting preparation and participate as appropriate
Set clinical data review strategy and lead collection and review of clinical data and trends
Review and query data and present relevant findings to internal and external stakeholders
Analyze emerging drug safety profiles with medically qualified colleagues and communicate changes to clinical and safety colleagues
Follow SOPs and regulations and lead or participate in workgroups optimizing clinical development procedures

Requirements

What you’ll need

PhD/Pharm D in a relevant Science discipline and minimum of 5 years Clinical Research experience in industry/CRO, OR MS in a relevant Science discipline and minimum of 7 years of Clinical Research experience in industry/CRO OR BA/BS in a relevant Science discipline and minimum of 10 years Clinical Research experience in a similar role in industry/CRO
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
Solid tumor or hematology clinical trial experience
Experience leading a team
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 through 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
This position requires permanent work authorization in the United States
U.S. work visa sponsorship is not available for this role now or in the future

Benefits

Comp & perks

Pfizer’s Global Performance Plan with a bonus target of 20.0% of base salary
Share based long term incentive program
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
Relocation assistance may be available based on business needs and/or eligibility