Hiring: Oncology Late Stage Clinical Scientist (Non-MD, Senior Manager)
📍 Locations:
United States: California (La Jolla, South San Francisco), Washington (Bothell), Pennsylvania (Collegeville), New York (New York City), Massachusetts (Cambridge), Connecticut (Groton)
💼 Job Type: Full-time
🆔 Job ID: 4944756
📅 Posted: 2 Days Ago
🌐 Work Arrangement: Hybrid – On-site ~2.5 days/week
About Pfizer
Pfizer is committed to breakthroughs that improve patient lives. Pfizer Research & Development drives innovation across therapeutic areas, including Oncology, ensuring safe, effective, and transformative medicines reach patients worldwide.
Position Summary
The Oncology Late Stage Clinical Scientist (Non-MD, Senior Manager) provides scientific oversight, ensures data integrity, and maintains quality for clinical trials in the Late-Stage Oncology portfolio. This role collaborates across clinical, medical, and operations teams to support successful clinical development and regulatory submissions.
Key Responsibilities
Clinical Expertise & Oversight
Serve as clinical development expert for assigned studies and maintain up-to-date knowledge in therapeutic and disease areas.
Ensure scientific oversight, quality, and integrity of clinical trials.
Set clinical data review strategy, lead quality data collection, and review emerging clinical data trends.
Collaborate with medically qualified colleagues on emerging safety profile analysis.
Study Design & Documentation
Author protocols, informed consent documents, site training materials, clinical study reports, and regulatory documents.
Contribute to Investigator Brochures and support Health Authority meetings.
Represent study teams in governance meetings and support Development Leads/Medical Directors on study and disease area strategy.
Collaboration & Cross-Functional Partnerships
Partner with clinical, medical, and operations teams to execute trials effectively.
Review and discuss data with internal and external stakeholders, governance bodies, and committees.
Participate in portfolio- and enterprise-level workgroups to optimize clinical development procedures.
Process & Quality Improvement
Follow SOPs and regulations while seeking opportunities to enhance clinical trial quality and efficiency.
Serve as subject matter expert or business process owner for relevant SOPs.
Embrace evolving technologies and best practices to improve clinical development processes.
Leadership & Team Development
Demonstrate autonomous delivery, agile decision-making, and problem-solving.
Promote team health, leadership behaviors, and effective collaboration across diverse, global teams.
Minimum Qualifications
Education:
PhD/PharmD + 2 years clinical research experience, OR
MS + 5 years clinical research experience, OR
BA/BS + 7 years clinical research experience in industry/CRO.
Experience:
Phase 3/pivotal Oncology clinical research experience, preferably on the sponsor side.
Knowledge of ICH guidelines, GCP, and FDA/EMA/global regulations.
Understanding of related disciplines: Clinical Operations, Safety, Biostatistics, Regulatory, Study Management, Pre-clinical, Pharmacology, QA.
Experience managing large data sets and authoring scientific publications, abstracts, or presentations.
Skills:
Proficiency in Microsoft Office and scientific software.
Effective communication, presentation, problem-solving, and organizational skills.
Ability to work independently, prioritize, and collaborate across teams.
Competencies for Success
Passion for oncology science and patient care.
Adaptability and resilience in a dynamic environment.
Autonomous delivery, agile decision-making, and problem-solving.
Global perspective and cultural awareness in diverse team settings.
Innovation, risk-taking, and continuous process improvement.
Leadership and ability to mentor, influence, and collaborate effectively.
Compensation & Benefits
Salary Range: $135,100 – $225,100 (U.S.)
Bonus: Eligible for Pfizer’s Global Performance Plan (17.5% target)
Benefits: 401(k) with matching contributions, retirement savings, paid vacation/holidays, medical, dental, vision, parental leave, and more.
Relocation: Assistance available based on business needs/eligibility.
Equal Opportunity
Pfizer is committed to equal opportunity and complies with all applicable laws regarding non-discrimination, work authorization, and accessibility. Permanent U.S. work authorization is required.
🔗 Apply Now: Pfizer Careers – Oncology Late Stage Clinical Scientist
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