Clinical Development Lead, Oncology/pathology

Roche UK

Tucson, Arizona, USA
Base: $120,500-$223,700; bonus/equity: discretiona...
Fully remote
Medical degree or advanced degree in life sciences
7+ years academic or diagnostics industry experience
Knowledge of fda ema pmda regulatory bodies
The role is responsible for planning and implementing clinical development activities for novel medical value diagnostic solutions in oncology and tissue-based pathology

Job Summary

  • The role is responsible for planning and implementing clinical development activities for novel medical value diagnostic solutions in oncology and tissue-based pathology.
  • Candidates must have a medical degree or advanced degree in Life Sciences, Oncology, Immunology, Molecular Biology, or Anatomic Pathology with at least 7 years of relevant experience.
  • Roche offers a competitive salary range of $120,500-$223,700 based on location, along with a discretionary annual bonus and comprehensive benefits.

Matching Summary

The role is responsible for planning and implementing clinical development activities for novel medical value diagnostic solutions in oncology and tissue-based pathology.

Salary

Base: $120,500-$223,700; Bonus/Equity: Discretionary annual bonus available; Benefits: Comprehensive benefits package detailed via link

Skills & Requirements

Must-have

  • Medical degree or advanced degree in Life Sciences
  • 7+ years academic or diagnostics industry experience
  • Knowledge of FDA EMA PMDA regulatory bodies
  • In-depth knowledge of ICH-GCP IVDD IVDR MDR regulations
  • Ability to align diagnostic test with cancer drug development

Nice-to-have

  • Experience working with pharmaceutical partners
  • Strong cross-functional collaboration skills
  • Ability to travel up to 10%
  • Leadership and coaching capabilities
  • Patient-centric mindset and behaviors

Key Requirements

  • Medical degree or PhD/PharmD in Life Sciences
  • 7+ years experience in diagnostics or pharma industry
  • Familiarity with global regulatory bodies like FDA and EMA
  • Understanding of IVD product development regulations
  • Ability to work independently in a matrixed environment

Work Rights

Not specified

Tailored Resume

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