Oncology Late Stage Clinical Scientist (senior Manager, Non Md)

Pfizer

Multiple Locations
Base: $139,100.00 - $231,900.00; bonus/equity: 17....
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Clinical trial scientific oversight
Data integrity and quality
Oncology late-stage portfolio
** Pfizer is seeking a Senior Manager for the Oncology Late Stage Clinical Scientist role, responsible for overseeing scientific integrity and quality in late-stage oncology clinical trials. The ideal candidate should possess relevant academic qualifications and substantial clinical research experience, particularly in oncology. **

Job Summary

  • Responsible for scientific oversight, data integrity, and quality of clinical trials in support of development strategy for the Late-Stage Oncology portfolio.
  • Author protocols, informed consent documents, and contribute to clinical study reports and regulatory documents, while supporting Health Authority meetings.
  • This is a Hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week.

Matching Summary

Match Score: 75

** Pfizer is seeking a Senior Manager for the Oncology Late Stage Clinical Scientist role, responsible for overseeing scientific integrity and quality in late-stage oncology clinical trials. The ideal candidate should possess relevant academic qualifications and substantial clinical research experience, particularly in oncology. **

Salary

Base: $139,100.00 - $231,900.00; Bonus/Equity: 17.5% bonus target; Benefits: Comprehensive benefits and programs including 401(k), paid time off, medical, dental, and vision coverage

Skills & Requirements

Must-have

  • clinical trial scientific oversight
  • data integrity and quality
  • Oncology late-stage portfolio
  • ICH guidelines and GCP
  • regulatory submissions and approvals

Nice-to-have

  • passion for helping patients
  • flexibility and adaptability
  • autonomous delivery and decision-making
  • global perspective and mindset

Key Requirements

  • PhD/PharmD with 2+ years experience OR MS with 5+ years experience OR BA/BS with 7+ years experience
  • Clinical Research experience in phase 3/pivotal Oncology
  • Experience with regulatory submissions and inspections
  • Excellent knowledge of clinical procedures, ICH guidelines, GCP, FDA, EMA regulations
  • Experience working on large data sets

Work Rights

Permanent work authorization in the United States

Tailored Resume

Cover Letter