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

539

Multiple Locations
Base: $282,200.00 - $444,200.00; bonus/equity: ann...
Hybrid
Clinical development strategies
Planning clinical trials
Medical oversight of trials
The Senior Clinical Director has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Late Stage Oncology - Late Stage therapeutic area

Job Summary

  • The Senior Clinical Director has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Late Stage Oncology - Late Stage therapeutic area.
  • The Senior Clinical Director may manage the entire cycle of clinical development for their assigned studies including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable, and offered a comprehensive package of benefits including medical, dental, vision, retirement, paid holidays, vacation, and sick days.

Matching Summary

The Senior Clinical Director has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Late Stage Oncology - Late Stage therapeutic area.

Salary

Base: $282,200.00 - $444,200.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Comprehensive package of benefits

Skills & Requirements

Must-have

  • Clinical development strategies
  • Planning clinical trials
  • Medical oversight of trials
  • Analyzing clinical findings
  • Maintaining scientific fund of knowledge
  • Engage with functional areas

Nice-to-have

  • Strong scientific scholarship
  • Interpersonal skills
  • Team environment
  • Intellectual curiosity
  • External research collaborations

Key Requirements

  • M.D or M.D./Ph.D. required
  • Minimum 3 years clinical medicine experience
  • Minimum 3 years industry drug development experience
  • Oversight of clinical studies and protocols
  • Board Certified or Eligible in Oncology preferred

Work Rights

Not specified

Tailored Resume

Cover Letter