Director, Clinical Development Scientist (non-md)

pfizer.de

Base: $176,600.00 to $294,300.00; bonus/equity: 20...
Hybrid
Clinical trial design and execution
Clinical data and safety review
Protocol development and amendments
The Director, Clinical Development Scientist is accountable for the scientific integrity of the study and the well-being of the patients enrolled in one or more clinical trials

Job Summary

  • The Director, Clinical Development Scientist is accountable for the scientific integrity of the study and the well-being of the patients enrolled in one or more clinical trials.
  • This role involves leading clinical execution of medium to high complexity studies, ensuring efficient protocol design, and partnering with global development leads on strategy and governance.
  • Pfizer offers a competitive salary range, bonus eligibility, share-based incentives, comprehensive benefits including retirement plans, paid leave, and health coverage.

Matching Summary

The Director, Clinical Development Scientist is accountable for the scientific integrity of the study and the well-being of the patients enrolled in one or more clinical trials.

Salary

Base: $176,600.00 to $294,300.00; Bonus/Equity: 20.0% bonus target plus share-based long term incentives; Benefits: comprehensive health, retirement, paid leave, and other benefits

Skills & Requirements

Must-have

  • clinical trial design and execution
  • clinical data and safety review
  • protocol development and amendments
  • risk management and mitigation
  • collaboration with clinical and medical teams
  • management of Data Monitoring Committees

Nice-to-have

  • leadership and team coaching
  • global and regional regulation knowledge
  • continuous improvement and process enhancement
  • matrix management support
  • effective communication with stakeholders

Key Requirements

  • Advanced degree or professional certification in healthcare or scientific discipline
  • 5+ years clinical research and development experience
  • Phase 3/pivotal clinical research experience
  • Extensive knowledge of ICH/GCP and adverse event management
  • Permanent US work authorization required

Work Rights

Permanent US work authorization required

Tailored Resume

Cover Letter