Clinical Development Medical Senior Director

Pfizer Com Ec

Unknown, ,
Base: $274,500.00 to $457,500.00; bonus/equity: 25...
**
Clinical development leadership
Protocol design and execution
Medical and scientific integrity
** Pfizer is seeking a Clinical Development Medical Senior Director who will lead innovative clinical development strategies, ensuring the integrity and well-being of trial participants. The ideal candidate will possess a medical degree, extensive experience in clinical research, and strong leadership skills in a biopharmaceutical environment. **

Job Summary

  • Leads innovative approaches to clinical development, develops and oversees implementation of solutions for complex problems with sustained and significant impact.
  • 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.
  • This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week, with a salary range of $274,500.00 to $457,500.00, eligible for bonus and long-term incentives.

Matching Summary

Match Score: 75

** Pfizer is seeking a Clinical Development Medical Senior Director who will lead innovative clinical development strategies, ensuring the integrity and well-being of trial participants. The ideal candidate will possess a medical degree, extensive experience in clinical research, and strong leadership skills in a biopharmaceutical environment. **

Salary

Base: $274,500.00 to $457,500.00; Bonus/Equity: 25.0% bonus target and share-based long-term incentive; Benefits: Comprehensive benefits package including 401(k), paid time off, medical, dental, and vision coverage

Skills & Requirements

Must-have

  • clinical development leadership
  • protocol design and execution
  • medical and scientific integrity
  • participant safety oversight
  • regulatory compliance management
  • stakeholder communication

Nice-to-have

  • innovative approach development
  • cross-functional team leadership
  • strategic development support
  • matrix management experience
  • global perspective and mindset

Key Requirements

  • MD, DO, MBBS, MBChB degree
  • 7+ years biopharmaceutical R&D experience
  • Licensed to prescribe medicines
  • Phase 3 clinical research experience
  • Demonstrated scientific writing skills
  • Global and regional regulation knowledge
  • ICH/GCP knowledge
  • Adverse event management knowledge
  • Clinical/medical project management capabilities
  • Excellent English communication skills
  • Experience establishing/managing/training teams

Work Rights

Permanent work authorization in the United States

Tailored Resume

Cover Letter