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: 4945569
Job Category: Clinical Development / Oncology / Late-Stage
Position Overview:
Pfizer is seeking a Senior Manager – Oncology Late-Stage Clinical Scientist (Non-MD) to provide scientific oversight, ensure data integrity, and maintain the quality of pivotal oncology clinical trials. This role supports late-stage development programs, collaborating with cross-functional teams to execute study strategies that drive clinical, regulatory, and operational success.
The ideal candidate will bring strong experience in Phase 3 oncology trials, demonstrate clinical and scientific expertise, and effectively translate emerging data into actionable insights. This position requires independent decision-making, leadership in study execution, and strong collaboration across global teams.
Key Responsibilities:
Clinical Oversight & Development
Serve as the clinical development expert for assigned oncology studies, staying current with therapeutic area knowledge and clinical advancements.
Ensure scientific oversight, data quality, and integrity of late-stage oncology trials.
Collaborate with clinical operations, medical colleagues, and other functional teams to ensure timely and efficient execution of trials.
Regulatory & Documentation Support
Author and review study protocols, informed consent documents, Investigator Brochures, clinical study reports, and regulatory submissions.
Support Health Authority meetings and ensure alignment with regulatory strategy.
Present emerging clinical and safety data to internal governance committees, study teams, and external stakeholders.
Data Analysis & Safety Monitoring
Lead clinical data review strategies and assess trends in safety and efficacy data.
Collaborate with medically qualified colleagues to monitor emerging safety profiles and communicate critical insights.
Ensure compliance with ICH-GCP guidelines, SOPs, and global regulations (FDA, EMA, and other health authorities).
Process Improvement & Leadership
Participate in enterprise-level workgroups and process optimization initiatives to enhance trial quality and efficiency.
Mentor junior team members and foster cross-functional collaboration.
Promote innovation and continuous improvement in clinical trial procedures and tools.
Minimum Qualifications:
PhD/PharmD with ≥2 years of clinical research experience in industry or CRO, OR
MS with ≥5 years of clinical research experience in industry or CRO, OR
BA/BS with ≥7 years of clinical research experience in a similar role in industry or CRO.
Proven experience in Phase 3/pivotal oncology trials, preferably sponsor-side, with a track record of successful regulatory submissions and approvals.
Strong knowledge of clinical procedures, ICH-GCP guidelines, and global regulatory standards.
Experience with large datasets, scientific software, and Microsoft Office suite.
Excellent communication, presentation, and organizational skills.
Preferred Qualifications:
Experience in Hematology Oncology or immuno-oncology.
Track record of publications, abstracts, posters, or presentations in clinical research.
Previous involvement in regulatory submissions, inspections, and approvals.
Competencies for Success:
Passion for oncology research and improving patient outcomes.
Ability to navigate dynamic, fast-paced environments while maintaining high-quality standards.
Autonomous decision-making, problem-solving, and agile execution of clinical responsibilities.
Global mindset and ability to collaborate effectively with culturally diverse teams.
Demonstrated leadership, influence, and ability to coach and guide colleagues for impactful results.
Work Arrangement:
Hybrid role; requires ~2.5 days onsite per week with 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 including 401(k) with company match, paid leave, parental leave, and medical, dental, and vision coverage.
Why Join Pfizer:
Join a global leader in oncology research, contributing to pivotal clinical trials and regulatory strategies that directly impact patient care worldwide. Influence late-stage development programs and collaborate across multidisciplinary teams to advance life-changing therapies.
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