Director, Clinical Development Scientist (non-md)

pfizer.ch

$176,600.00 - $294,300.00; bonus target of 20.0%; ...
Hybrid (2.5 days onsite per week)
Scientific integrity of study
Patient well-being
Protocol development
Pfizer is seeking a Director, Clinical Development Scientist to oversee the scientific integrity of clinical trials, ensuring high-quality execution and compliance. The role demands extensive clinical research experience, particularly in phase 3 trials, and offers a hybrid work environment with comprehensive benefits

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.
  • The role applies technical and clinical skills to ensure the design of efficient and high-quality clinical trials, employing quantitative design principles, and clinical best practices to deliver both clinical and operational excellence.
  • We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.

Matching Summary

Match Score: 85

Pfizer is seeking a Director, Clinical Development Scientist to oversee the scientific integrity of clinical trials, ensuring high-quality execution and compliance. The role demands extensive clinical research experience, particularly in phase 3 trials, and offers a hybrid work environment with comprehensive benefits.

Salary

$176,600.00 - $294,300.00; Bonus target of 20.0%; Comprehensive benefits

Skills & Requirements

Must-have

  • scientific integrity of study
  • patient well-being
  • protocol development
  • clinical trial execution
  • data interpretation and communication
  • risk mitigation

Nice-to-have

  • cardiometabolic disease experience
  • leadership and coaching
  • influencing and collaboration

Key Requirements

  • Advanced degree or professional certification
  • 5+ years of experience in clinical research and development
  • Phase 3/pivotal clinical research experience
  • Extensive knowledge of clinical development, global and regional regulation, ICH/GCP, adverse event management
  • Demonstrated clinical, administrative, and project management capabilities
  • Excellent verbal and written communication skills in English
  • Demonstrated experience establishing, managing, and training teams

Work Rights

Permanent work authorization in the United States

Tailored Resume

Cover Letter