Senior Medical Director, Clinical Research (oncology)

Sumitomo Pharma Co., Ltd.

Remote
Base: $284,320 - $355,400; bonus/equity: short inc...
Fully remote
Lead clinical development program design
Oversee investigator education
Manage clinical study teams
Sumitomo Pharma Co., Ltd. is seeking a Senior Medical Director for Clinical Research in Oncology, responsible for leading clinical studies and collaborating with key stakeholders in the pharmaceutical industry. The position requires extensive experience in drug development and a strong medical background

Job Summary

  • The Senior Medical Director is responsible for the leadership, development, and management of clinical studies while building and maintaining relationships with investigators and key opinion leaders.
  • Contribute to company’s planned regulatory filings including authoring clinical sections for INDs, NDAs, and other related documents.
  • The base salary range for this role is $284,320 to $355,400, part of a total rewards package.

Matching Summary

Match Score: 85

Sumitomo Pharma Co., Ltd. is seeking a Senior Medical Director for Clinical Research in Oncology, responsible for leading clinical studies and collaborating with key stakeholders in the pharmaceutical industry. The position requires extensive experience in drug development and a strong medical background.

Salary

Base: $284,320 - $355,400; Bonus/Equity: Short incentive plan participation; Benefits: Medical, dental, vision, life and disability insurances, 401(k) plan, flexible paid time off, 11 paid holidays, year-end shut down, 80 hours paid sick time

Skills & Requirements

Must-have

  • Lead clinical development program design
  • Oversee investigator education
  • Manage clinical study teams
  • Review and interpret safety data
  • Present at global scientific meetings
  • Author clinical regulatory filings
  • Assess compound safety profiles

Nice-to-have

  • Build investigator relationships
  • Collaborate with thought leaders
  • Contribute to due diligence

Key Requirements

  • Medical Doctor (MD), Doctor of Osteopathy (DO), or non-US equivalent
  • Completion of a residency program strongly preferred
  • Completion of a subspecialty fellowship is desirable
  • Experience in the treatment and management of myelofibrosis is recommended
  • 5-10 years of pharmaceutical drug development experience

Work Rights

Not specified

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