Executive Director, Clinical Development Program Lead (neuropsychiatry)

Bristor Myers Squibb

Multiple Locations
Base: $340,870 - $413,051; bonus/equity: + incenti...
50% onsite
Clinical development strategy
Clinical trial design and execution
Regulatory filings
The Clinical Development Program Leader will set the clinical development strategy for assets or indications and directly supervise the work of multiple Clinical Development Leads

Job Summary

  • The Clinical Development Program Leader will set the clinical development strategy for assets or indications and directly supervise the work of multiple Clinical Development Leads.
  • This role will include above disease / indication strategy work, supervising broad Clinical Development teams across several Development teams, as well as Disease / Indication Strategy teams.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

The Clinical Development Program Leader will set the clinical development strategy for assets or indications and directly supervise the work of multiple Clinical Development Leads.

Salary

Base: $340,870 - $413,051; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • Clinical development strategy
  • Clinical trial design and execution
  • Regulatory filings
  • Neuropsychiatry drug development
  • Leadership of clinical development teams

Nice-to-have

  • Attracts innovators
  • Values diversity of thought
  • Process excellence and continuous improvement
  • External thought leader engagement

Key Requirements

  • MD required
  • Greater than 10 years of clinical trial experience
  • Greater than 10 years of drug development experience
  • Greater than 10 years of regulatory experience
  • Management experience required
  • Experience designing Phase I, II, and III clinical trials
  • Demonstrable success filing regulatory dossiers

Work Rights

Not specified

Tailored Resume

Cover Letter