Executive Director, Product Development Team Leader, Clinical Research, Hematology - Lymphoma

Merck & Co., Inc.

Base: $310,900.00 - $489,400.00; bonus/equity: ann...
Hybrid
3 years clinical medicine experience
5 years industry drug development experience
Authoring regulatory documents
The Executive Director will oversee the entire cycle of late-stage clinical development from Phase 2 to Phase 5 for new and marketed medicines in the Oncology therapeutic area

Job Summary

  • The Executive Director will oversee the entire cycle of late-stage clinical development from Phase 2 to Phase 5 for new and marketed medicines in the Oncology therapeutic area.
  • This role requires leading cross-functional product development teams to execute program strategies while interacting with key scientific leaders externally.
  • The successful candidate will be eligible for an annual bonus, long-term incentives, and a comprehensive benefits package including medical, dental, vision, and 401(k) retirement plans.

Matching Summary

The Executive Director will oversee the entire cycle of late-stage clinical development from Phase 2 to Phase 5 for new and marketed medicines in the Oncology therapeutic area.

Salary

Base: $310,900.00 - $489,400.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • 3 years clinical medicine experience
  • 5 years industry drug development experience
  • Authoring regulatory documents
  • Leading cross-functional product teams
  • Phase 2 to Phase 5 clinical trial management

Nice-to-have

  • Board certified in Oncology or Hematology
  • Prior lymphoma therapeutic area experience
  • Strong publication record in scientific scholarship
  • Product registration experience
  • Ability to travel 20 percent of the time

Key Requirements

  • M.D. or M.D./Ph.D. degree required
  • Minimum 3 years clinical medicine experience
  • Minimum 5 years industry drug development experience
  • Demonstrated success in protocol authoring and regulatory discussions
  • Proven track record in biomedical research

Work Rights

Not specified

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