Clinical Development Medical Senior Director

Data Science Jobs

Base: $274,500.00 - $457,500.00; bonus/equity: 25....
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Clinical development strategy
Protocol design and execution
Medical monitoring
** The Clinical Development Medical Senior Director role at Pfizer involves leading innovative clinical development approaches and overseeing complex clinical trials. The ideal candidate should have extensive medical qualifications and experience in clinical research, with a focus on ensuring medical integrity and compliance throughout study execution. **

Job Summary

  • Leads innovative approaches to clinical development, develops and oversees implementation of solutions for complex problems with sustained and significant impact, and acts as subject matter expert for clinical development, influencing the decisions of senior leaders.
  • Ensures medical & scientific integrity and the wellbeing of participants enrolled in clinical trials, designs and executes high-quality studies, maintains compliance, manages risks and emerging clinical and medical issues, and supports interpretation and communication of clinical data.
  • The annual base salary for this position ranges from $274,500.00 to $457,500.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 25.0% of the base salary and eligibility to participate in our share based long term incentive program.

Matching Summary

Match Score: 75

** The Clinical Development Medical Senior Director role at Pfizer involves leading innovative clinical development approaches and overseeing complex clinical trials. The ideal candidate should have extensive medical qualifications and experience in clinical research, with a focus on ensuring medical integrity and compliance throughout study execution. **

Salary

Base: $274,500.00 - $457,500.00; Bonus/Equity: 25.0% bonus target; Benefits: Comprehensive and generous benefits

Skills & Requirements

Must-have

  • clinical development strategy
  • protocol design and execution
  • medical monitoring
  • safety data review
  • regulatory filings support
  • cross-functional team leadership

Nice-to-have

  • influence senior leaders
  • innovative approaches
  • participant wellbeing
  • global perspective
  • agile decision-making

Key Requirements

  • MD, DO, MBBS, MBChB degree
  • 7+ years biopharmaceutical industry experience
  • Licensed to prescribe medicines
  • Phase 3/pivotal clinical research experience
  • Demonstrated scientific writing skills
  • Global and regional regulation knowledge
  • ICH/GCP knowledge
  • Adverse event management knowledge

Work Rights

Permanent work authorization required

Tailored Resume

Cover Letter