Executive Medical Director, Clinical Development, Breast Cancer

Menarini Group

Remote, US
Base: $300,000 - $400,000; bonus/equity: annual bo...
Remote
12+ years pharma/biotech experience
Phase i-iv clinical development strategy
Oncology product regulatory submission experience
The Menarini Group is seeking an Executive Medical Director for Clinical Development in Breast Cancer, responsible for leading the global clinical strategy for their Elacestrant product. This remote position requires a medical degree, extensive oncology experience, and expertise in clinical trial development

Job Summary

  • The Executive Medical Director will drive the global clinical development strategy for Stemline's Breast Cancer product, Elacestrant, including a pivotal Phase 3 study.
  • This role requires leading multi-disciplinary teams to guide clinical development, manage regulatory submissions, and ensure robust study conduct across Phase 1 through 4 trials.
  • Menarini Stemline offers a base salary range of $300,000 - $400,000 plus annual bonus and long-term incentives along with comprehensive benefits packages.

Matching Summary

Match Score: 85

The Menarini Group is seeking an Executive Medical Director for Clinical Development in Breast Cancer, responsible for leading the global clinical strategy for their Elacestrant product. This remote position requires a medical degree, extensive oncology experience, and expertise in clinical trial development.

Salary

Base: $300,000 - $400,000; Bonus/Equity: Annual bonus & long-term Incentives; Benefits: Fidelity 401(k) match, Anthem insurance, Basic Life & AD&D, FSA/HSA

Skills & Requirements

Must-have

  • 12+ years pharma/biotech experience
  • Phase I-IV clinical development strategy
  • Oncology product regulatory submission experience
  • Board certified oncologist or oncology training
  • Breast Cancer compound development experience

Nice-to-have

  • Leadership of medical and scientific directors
  • Experience with innovative clinical strategies
  • Ability to work in fast-paced environment
  • Strong peer recognition in scientific community
  • Comfortable with ambiguity and self-motivated

Key Requirements

  • Medical Degree required
  • 12+ years pharmaceutical industry experience
  • Board certification in oncology preferred
  • Proven track record of successful regulatory submissions
  • Working knowledge of GCP, ICH, FDA, and EMEA regulations

Work Rights

Not specified

Tailored Resume

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