Clinical Development Scientist, Director

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Multiple Locations
Base: $176,600.00 to $294,300.00; bonus/equity: 20...
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Clinical trial execution leadership
Clinical protocol development
Clinical safety and risk management
** The Clinical Development Scientist, Director position at Pfizer involves leading clinical studies, ensuring scientific integrity, and maintaining compliance throughout the clinical trial process. Candidates are expected to have extensive experience in clinical research, particularly in the biopharmaceutical industry, with a strong focus on regulatory compliance and project management. **

Job Summary

  • The Clinical Development Scientist (Director) ensures scientific integrity and participant safety in clinical trials while leading medium to high complexity studies with significant business impact.
  • This role offers a hybrid work model with comprehensive benefits including a 401(k) plan with matching contributions, paid leave, and health coverage, along with a competitive salary and bonus structure.
  • Pfizer is committed to equal opportunity employment and requires permanent work authorization in the United States without visa sponsorship.

Matching Summary

Match Score: 75

** The Clinical Development Scientist, Director position at Pfizer involves leading clinical studies, ensuring scientific integrity, and maintaining compliance throughout the clinical trial process. Candidates are expected to have extensive experience in clinical research, particularly in the biopharmaceutical industry, with a strong focus on regulatory compliance and project management. **

Salary

Base: $176,600.00 to $294,300.00; Bonus/Equity: 20% bonus target plus share-based long term incentives; Benefits: comprehensive health, retirement, paid leave and other benefits

Skills & Requirements

Must-have

  • clinical trial execution leadership
  • clinical protocol development
  • clinical safety and risk management
  • clinical data review and reporting
  • stakeholder communication and collaboration
  • clinical regulatory compliance
  • matrix management support

Nice-to-have

  • oncology experience
  • global and diverse team collaboration
  • scientific writing skills
  • analytical skills with large data sets
  • adaptability in changing environments
  • problem-solving and agile decision-making
  • innovation and process improvement

Key Requirements

  • Advanced degree in health care or scientific discipline
  • 5+ years clinical research experience with PhD/PharmD
  • Clinical research experience in phase 3/pivotal trials
  • Extensive knowledge of ICH/GCP and adverse event management
  • Demonstrated leadership and project management skills
  • Permanent US work authorization required
  • No US visa sponsorship available

Work Rights

Permanent US work authorization required

Tailored Resume

Cover Letter