Senior Principal Scientist, Clinical Research, Endometrial Cancer

Merck Sharp & Dohme Corp

Multiple Locations, US
Base: $282,200.00 - $444,200.00; bonus/equity: ann...
Hybrid (3 days onsite, 1 day remote)
Clinical development strategy
Medical oversight of trials
Oncology therapeutic area expertise
Merck Sharp & Dohme Corp is seeking a Senior Principal Scientist for Clinical Research in Endometrial Cancer, responsible for leading clinical research activities and overseeing the entire clinical development cycle for oncology medicines. The ideal candidate will have a substantial background in clinical medicine and drug development, with expertise in oncology research, and will work in a hybrid model

Job Summary

  • The Senior Clinical Director is responsible for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area.
  • This role requires developing clinical development strategies for investigational or marketed drugs specifically in Endometrial Cancer and providing medical oversight of ongoing trials.
  • The company offers a comprehensive benefits package including medical, dental, vision, retirement benefits, and paid holidays alongside a salary range of $282,200.00 to $444,200.00.

Matching Summary

Match Score: 85

Merck Sharp & Dohme Corp is seeking a Senior Principal Scientist for Clinical Research in Endometrial Cancer, responsible for leading clinical research activities and overseeing the entire clinical development cycle for oncology medicines. The ideal candidate will have a substantial background in clinical medicine and drug development, with expertise in oncology research, and will work in a hybrid model.

Salary

Base: $282,200.00 - $444,200.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • Clinical development strategy
  • Medical oversight of trials
  • Oncology therapeutic area expertise
  • Endometrial cancer focus
  • Regulatory reporting experience

Nice-to-have

  • Cross-functional collaboration skills
  • Scientific scholarship record
  • External investigator networking
  • Business development assessment
  • Strategic planning capabilities

Key Requirements

  • M.D. or M.D./Ph.D. degree required
  • Minimum 3 years industry experience in drug development
  • Board Certified or Eligible in oncology/hematology preferred
  • Prior specific experience in clinical research and publication required

Work Rights

Not specified

Tailored Resume

Cover Letter