Oncology Late Stage Clinical Development Scientist (non Md, Director)

pfizer.co.ke

Base: $176,600.00 - $282,900.00; bonus/equity: 20....
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Late-stage oncology portfolio
Scientific oversight
Data integrity and quality
** Pfizer is seeking an Oncology Late Stage Clinical Development Scientist (non-MD, Director) to oversee scientific integrity and quality in late-stage oncology clinical trials. The ideal candidate should possess significant clinical research experience in oncology, with a focus on regulatory submissions and collaboration across multiple teams. **

Job Summary

  • You will be 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.
  • The annual base salary for this position ranges from $176,600.00 to $282,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program.

Matching Summary

Match Score: 75

** Pfizer is seeking an Oncology Late Stage Clinical Development Scientist (non-MD, Director) to oversee scientific integrity and quality in late-stage oncology clinical trials. The ideal candidate should possess significant clinical research experience in oncology, with a focus on regulatory submissions and collaboration across multiple teams. **

Salary

Base: $176,600.00 - $282,900.00; Bonus/Equity: 20.0% bonus target; Benefits: Comprehensive and generous benefits

Skills & Requirements

Must-have

  • Late-Stage Oncology portfolio
  • scientific oversight
  • data integrity and quality
  • protocol authoring
  • clinical data review strategy
  • ICH guidelines
  • GCP compliance

Nice-to-have

  • passion for helping patients
  • agile decision-making
  • innovation and risk-taking
  • global perspective and mindset
  • leading direct reports

Key Requirements

  • PhD/Pharm D with 5 years clinical research experience OR MS with 7 years experience OR BA/BS with 10 years experience
  • Phase 3/pivotal space Oncology experience
  • Sponsor-side experience
  • Track record of successful regulatory submission
  • Familiarity with FDA, EMA, and global regulations
  • Permanent work authorization in the United States

Work Rights

Permanent work authorization

Tailored Resume

Cover Letter