Director Clinical Development, Solid Tumors

beigene.at

$249,800.00 - $309,800.00 annually; bonus/equity: ...
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Clinical development programs
Execution of clinical studies
Global clinical study design
** Beigene is seeking a Director of Clinical Development for Solid Tumors to lead and execute clinical development programs aimed at combating cancer. The ideal candidate will possess a medical degree, significant oncology experience, and a strong background in clinical trial management. **

Job Summary

  • The Director, Clinical Development will support BeOne Clinical and Medical assets by successful execution of clinical development programs and deliverables in partnership across the organization.
  • The incumbent will play a key role the establishment and growth of Clinical Research functions to assure best-in-class global capabilities and execution.
  • The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

Matching Summary

Match Score: 75

** Beigene is seeking a Director of Clinical Development for Solid Tumors to lead and execute clinical development programs aimed at combating cancer. The ideal candidate will possess a medical degree, significant oncology experience, and a strong background in clinical trial management. **

Salary

$249,800.00 - $309,800.00 annually; Bonus/Equity: Eligible for annual bonus plan/incentive compensation plan and discretionary equity awards; Benefits: Comprehensive benefits package

Skills & Requirements

Must-have

  • Clinical development programs
  • Execution of clinical studies
  • Global clinical study design
  • Drug development process
  • GCP and ICH Guidelines
  • Scientific and medical support

Nice-to-have

  • Values based collaborator
  • Strategic and creative thinker
  • Impactful written and verbal communication
  • Problem solving and risk-mitigation
  • Appreciation of diversity and multiculturalism

Key Requirements

  • MD or DO or international equivalent degree
  • 5 plus years of experience
  • Previous participation in clinical development program
  • Clinical oncology experience
  • Expert understanding of global clinical study design

Work Rights

Not specified

Tailored Resume

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