Senior Principal Scientist (senior Director), Clinical Research, Adc

Merck & Co., Inc.

Rahway, NJ, USA
Base: $282,200.00 - $444,200.00; bonus/equity: ann...
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Oncology therapeutic area expertise
Clinical trial design and execution
Regulatory reporting and compliance
** Merck & Co., Inc. is seeking a Senior Principal Scientist (Senior Clinical Director) for its Oncology Asset therapeutic area, responsible for overseeing clinical research activities of new medicines. The ideal candidate will have substantial experience in drug development and clinical medicine, with a focus on Antibody Drug Conjugates (ADC). **

Job Summary

  • The Senior Clinical Director has primary responsibility for planning and directing clinical research activities involving new medicines in the Oncology Asset therapeutic area.
  • The role involves developing clinical development strategies, overseeing dose optimization studies, and analyzing clinical findings to support safety and efficacy decisions.
  • The company offers a comprehensive benefits package including medical, dental, vision, 401(k), and an annual bonus eligibility for this hybrid role.

Matching Summary

Match Score: 75

** Merck & Co., Inc. is seeking a Senior Principal Scientist (Senior Clinical Director) for its Oncology Asset therapeutic area, responsible for overseeing clinical research activities of new medicines. The ideal candidate will have substantial experience in drug development and clinical medicine, with a focus on Antibody Drug Conjugates (ADC). **

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

  • Oncology therapeutic area expertise
  • Clinical trial design and execution
  • Regulatory reporting and compliance
  • Drug development strategy planning
  • Medical oversight of clinical studies

Nice-to-have

  • Strong interpersonal and team skills
  • Experience with cross-functional collaboration
  • Ability to travel 20-25 percent of time
  • Scientific scholarship and publication record
  • Expert opinion on scientific questions

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 preferred
  • Prior specific experience in clinical research and publication
  • US and Puerto Rico residents only

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter