Oncology Late-Stage Clinical Scientist (Senior Manager, Non-MD)
Locations:
United States – Pennsylvania, Collegeville
United States – California, La Jolla
United States – Massachusetts, Cambridge
United States – Washington, Bothell
United States – Connecticut, Groton
Employment Type: Full-Time
Posted: 14 Days Ago
Job Requisition ID: 4945579
Job Category: Clinical Development / Oncology / Late-Stage
Role Summary:
Pfizer is seeking a Senior Manager – Oncology Late-Stage Clinical Scientist (Non-MD) to oversee the scientific integrity, data quality, and strategic execution of late-stage oncology clinical trials. This role ensures adherence to Pfizer’s development strategy for pivotal studies, providing cross-functional leadership and clinical expertise to advance therapies from Phase 3 to regulatory submission.
Key Responsibilities:
Clinical Expertise & Oversight
Serve as a clinical development expert for assigned oncology studies, maintaining current knowledge of disease area, therapies, and regulatory landscape.
Ensure scientific oversight, data integrity, and quality of clinical trials within the late-stage oncology portfolio.
Collaborate with medical, clinical operations, and functional teams to implement trials successfully and efficiently.
Partner with Development Leads and Medical Directors to define study strategy, regulatory submissions, and governance deliverables.
Documentation & Regulatory Support
Author clinical protocols, informed consent documents, Investigator Brochures, clinical study reports, and regulatory submissions.
Support Health Authority meetings and provide guidance on emerging clinical and safety data.
Implement clinical data review strategies and present findings to internal and external stakeholders.
Data Analysis & Safety Monitoring
Lead the review and analysis of clinical data, identifying trends and ensuring timely reporting.
Monitor emerging safety profiles in close collaboration with medically qualified colleagues.
Provide actionable insights to optimize study performance, patient safety, and regulatory compliance.
Process Improvement & Compliance
Ensure compliance with ICH guidelines, GCP standards, and global regulations (FDA, EMA, and other Health Authorities).
Actively contribute to process improvement initiatives, SOP enhancements, and enterprise-level best practices.
Leverage technology and data management tools to enhance operational efficiency and study quality.
Leadership & Collaboration
Mentor junior colleagues and foster team effectiveness across cross-functional teams.
Build strong internal partnerships to achieve program objectives and strategic outcomes.
Demonstrate leadership and influence in multi-cultural and global team environments.
Minimum Qualifications:
PhD/PharmD with ≥2 years clinical research experience in industry/CRO, OR
MS with ≥5 years clinical research experience in industry/CRO, OR
BA/BS with ≥7 years clinical research experience in a similar role in industry/CRO.
Proven experience in Phase 3/pivotal oncology trials, sponsor-side preferred, with successful regulatory submissions.
Strong understanding of clinical procedures, ICH-GCP guidelines, and regulatory requirements.
Experience with large clinical datasets and proficiency in Microsoft Office and relevant scientific software.
Excellent communication, presentation, and organizational skills.
Preferred Qualifications:
Experience in Hematology Oncology or immuno-oncology.
Track record of scientific productivity (publications, abstracts, posters, presentations).
Prior exposure to regulatory submissions, inspections, and approvals.
Competencies for Success:
Passion for oncology and improving patient outcomes.
Flexibility and adaptability in dynamic clinical research environments.
Strong autonomous decision-making, problem-solving, and agile execution skills.
Global mindset with the ability to collaborate across cultures, geographies, and functions.
Leadership skills to influence, mentor, and drive high-impact clinical initiatives.
Work Arrangement:
Hybrid role, requiring onsite presence ~2.5 days per week and commuting proximity to office locations.
Compensation & Benefits:
Annual base salary: $139,100 – $225,100
Eligible for Pfizer Global Performance Plan (17.5% bonus target) and share-based long-term incentives.
Comprehensive benefits include 401(k) with company match, vacation, paid leave, parental leave, and medical, dental, and vision coverage.
Why Join Pfizer:
Drive late-stage oncology innovation with a global leader in biopharmaceuticals. Influence clinical trial strategy, contribute to regulatory success, and support therapies that improve patient lives worldwide.
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