Executive Director, Companion Diagnostics

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Base: $210,400.00 - $331,100.00; bonus/equity: eli...
Hybrid (3 days onsite per week, remote on fridays)
Companion diagnostics (cdx) development
Biomarker platform expertise (ngs, ihc, pcr)
Regulatory document preparation
The Executive Director for Companion Diagnostics will lead a Diagnostic Development Team, overseeing strategy and execution for various oncology-related projects. The role requires extensive industry experience, particularly in biomarker development and regulatory processes, alongside strong leadership and communication skills

Job Summary

  • Lead cross-functional teams to drive CDx strategy, development, and implementation for a portfolio of assets/biomarkers, primarily in Oncology.
  • Supervise PhD-/MD-level employees leading diagnostic projects and coordinate work with external Dx partners.
  • The company offers a comprehensive package of benefits including medical, dental, vision, retirement, paid holidays, and vacation.

Matching Summary

Match Score: 85

The Executive Director for Companion Diagnostics will lead a Diagnostic Development Team, overseeing strategy and execution for various oncology-related projects. The role requires extensive industry experience, particularly in biomarker development and regulatory processes, alongside strong leadership and communication skills.

Salary

Base: $210,400.00 - $331,100.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Comprehensive package including medical, dental, vision, 401(k), paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • Companion Diagnostics (CDx) development
  • Biomarker platform expertise (NGS, IHC, PCR)
  • Regulatory document preparation
  • Cross-functional team leadership
  • Global regulatory agencies interaction

Nice-to-have

  • Deep technical knowledge in focus areas
  • Experience in both pharma and Dx settings
  • Digital pathology expertise

Key Requirements

  • PhD Required
  • Minimum 8 years of industry experience
  • Demonstrated track record in CDx development and approval
  • Experience with global CDx regulatory requirements (EU IVDR, China HGRAC, Japan PMDA)

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter