Director / Senior Director, Precision Diagnostics - Oncology

GSK

United States
Base: $189,750 to $316,250; bonus/equity: annual b...
Hybrid
8+ years diagnostic development experience
2-3 years oncology diagnostic experience
Clinical trial design and biomarker selection
This role involves implementing diagnostic development strategies that align with oncology development needs to treat the right patient with the right medicine

Job Summary

  • This role involves implementing diagnostic development strategies that align with oncology development needs to treat the right patient with the right medicine.
  • The successful candidate will oversee project plans, budgets, and timelines while ensuring compliance with FDA and EU medical device regulations.
  • GSK offers a hybrid work model, competitive salary ranges up to $316,250, and comprehensive benefits including health care and retirement plans.

Matching Summary

This role involves implementing diagnostic development strategies that align with oncology development needs to treat the right patient with the right medicine.

Salary

Base: $189,750 to $316,250; Bonus/Equity: Annual bonus and share-based long term incentive program; Benefits: Health care, retirement, paid holidays, vacation, and parental leave

Skills & Requirements

Must-have

  • 8+ years diagnostic development experience
  • 2-3 years oncology diagnostic experience
  • Clinical trial design and biomarker selection
  • FDA and EU medical device regulatory knowledge
  • Cross-functional project management skills
  • Stakeholder management with external partners

Nice-to-have

  • Next-generation sequencing (NGS) assay development
  • Experience with PCR or immunohistochemistry assays
  • Regulatory submission contribution history
  • Laboratory accreditation standards familiarity
  • Commercial team partnership for market adoption
  • Advanced degree in relevant discipline

Key Requirements

  • Bachelor's degree in life sciences or related field
  • 8 years of experience in diagnostic development
  • Knowledge of ISO13485 and GMP manufacturing
  • Proven ability to manage matrix environment projects

Work Rights

Not specified

Tailored Resume

Cover Letter