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 mission 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 mission to positively impact the health of 2.5 billion people by the end of the decade.
  • Candidates will lead cross-functional teams to define diagnostic requirements, oversee project plans, and ensure high-quality delivery of diagnostic milestones for oncology programs.
  • This hybrid position offers competitive compensation ranging from $189,750 to $316,250 annually, along with an annual bonus, long-term incentives, and comprehensive benefits.

Matching Summary

The role involves implementing diagnostic development strategies that align with GSK's mission 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 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 or immunohistochemistry assay development
  • Regulatory submission interactions
  • Commercial team partnership for launch
  • Laboratory accreditation standards familiarity
  • Advanced degree in life sciences

Key Requirements

  • Bachelor's degree in life sciences or related field
  • 8+ years in diagnostic development and biomarker strategy
  • Knowledge of FDA and EU medical device regulations
  • Experience with ISO13485 and QSR regulations
  • Proven ability to manage budgets and timelines

Work Rights

Not specified

Tailored Resume

Cover Letter