Medical Director, Hematology

BeOne Medicines

Base: $249,800.00 - $309,800.00 annually; bonus/eq...
Not specified
Md or equivalent medical degree required
Board certification in oncology or hematology
Experience across phases i-iii clinical trials
BeOne Medicines is seeking a Medical Director for Hematology to lead clinical development programs and collaborate with internal and external partners in the fight against cancer. The ideal candidate should have a strong background in clinical research, drug development, and excellent leadership skills, along with an MD or equivalent medical degree. The role offers competitive compensation and a comprehensive benefits package

Job Summary

  • The Medical Director will lead the execution of clinical development programs for BeOne's hematology assets while ensuring activities stay within scope, budget, and timelines.
  • This role requires authoring key regulatory documents such as protocols, Investigator Brochures, and Clinical Study Reports while providing scientific expertise to select investigators and vendors.
  • Candidates will benefit from a comprehensive benefits package including medical, dental, vision, 401(k), and discretionary equity awards alongside an annual bonus plan.

Matching Summary

Match Score: 85

BeOne Medicines is seeking a Medical Director for Hematology to lead clinical development programs and collaborate with internal and external partners in the fight against cancer. The ideal candidate should have a strong background in clinical research, drug development, and excellent leadership skills, along with an MD or equivalent medical degree. The role offers competitive compensation and a comprehensive benefits package.

Salary

Base: $249,800.00 - $309,800.00 annually; Bonus/Equity: Eligible for annual bonus plan and discretionary equity awards; Benefits: Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off

Skills & Requirements

Must-have

  • MD or equivalent medical degree required
  • Board certification in oncology or hematology
  • Experience across Phases I-III clinical trials
  • Deep knowledge of GCP and regulatory submissions
  • Safety oversight including DSURs and PSURs

Nice-to-have

  • Translational medicine and biomarker strategy experience
  • Global clinical trial experience across multiple geographies
  • Life cycle management and commercial interfacing skills
  • PK/PD data integration expertise
  • Proven track record in therapeutic area development

Key Requirements

  • MD (or equivalent medical degree)
  • Board certification in oncology or hematology
  • Clinical training with drug development experience
  • Demonstrated safety oversight skills
  • Strong understanding of IND, NDA, BLA regulations

Work Rights

Not specified

Tailored Resume

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