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 integration
The role involves implementing diagnostic development strategies that align with GSK's ambition to positively impact the health of 2.5 billion people by the end of the decade

Job Summary

  • The role involves implementing diagnostic development strategies that align with GSK's ambition to positively impact the health of 2.5 billion people by the end of the decade.
  • You will lead cross-functional teams to define diagnostic requirements, validate assays, and ensure on-time delivery of high-quality diagnostic milestones for oncology trials.
  • This hybrid position offers competitive compensation including an annual bonus, share-based long-term incentives, and comprehensive benefits such as health care and paid leave.

Matching Summary

The role involves implementing diagnostic development strategies that align with GSK's ambition to positively impact the health of 2.5 billion people by the end of the decade.

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 caregiver/parental leave

Skills & Requirements

Must-have

  • 8 years diagnostic development experience
  • 2-3 years oncology diagnostic experience
  • Clinical trial design integration
  • FDA and EU medical device regulations
  • Cross-functional project management
  • Biomarker strategy and assay validation

Nice-to-have

  • Next-generation sequencing (NGS) experience
  • PCR and immunohistochemistry expertise
  • Regulatory submission interactions
  • Commercial team partnership for launch
  • Curiosity, humility, and patient-first mindset

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Advanced degree (MS, PhD, MD) preferred
  • Knowledge of ISO13485 and QSR regulations
  • Experience with human biological specimen management
  • Proven ability to manage budgets and timelines

Work Rights

Not specified

Tailored Resume

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