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

Pfizer

Unknown, Unknown, Unknown
Base: $139,100.00 - $231,900.00; bonus/equity: 17....
Hybrid
Scientific oversight of clinical trials
Data integrity and quality
Oncology late-stage development
Responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio

Job Summary

  • Responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio.
  • Author protocols, study level informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents.
  • 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

Responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio.

Salary

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

Skills & Requirements

Must-have

  • Scientific oversight of clinical trials
  • Data integrity and quality
  • Oncology late-stage development
  • Protocol and document authoring
  • Clinical data review strategy
  • ICH guidelines and GCP compliance

Nice-to-have

  • Passion for helping patients with cancer
  • Autonomous delivery and agile decision-making
  • Promotes team health and leadership behaviors
  • Innovation and risk-taking
  • Global perspective and mindset

Key Requirements

  • PhD/PharmD with 2+ years industry/CRO clinical research experience
  • MS with 5+ years industry/CRO clinical research experience
  • BA/BS with 7+ years industry/CRO clinical research experience
  • Phase 3/pivotal oncology clinical research experience
  • Track record of successful regulatory submission/approval
  • Familiarity with FDA, EMA, and global regulations

Work Rights

Permanent work authorization in the United States

Tailored Resume

Cover Letter