Senior Director, Clinical Study Management

Abbott

Santa Clara, California, United States
Base: $218,700.00 – $437,300.00; bonus/equity: not...
Hybrid
Leading large-scale pre-market clinical trials
Managing global studies and large budgets
Influencing study design for operational feasibility
Abbott is seeking a Senior Director of Clinical Study Management to oversee a global portfolio of over 100 clinical studies within its Medical Devices division. The role requires a strategic leader with extensive experience in managing large-scale clinical trials and a strong understanding of global regulatory landscapes

Job Summary

  • This role involves leading a mission-driven portfolio of over 100 clinical studies impacting patient lives globally.
  • The position requires managing complex multi-business unit portfolios with budgets exceeding $100 million while ensuring operational excellence.
  • Abbott offers extensive benefits including free medical coverage, high employer retirement contributions, and tuition reimbursement programs.

Matching Summary

Match Score: 85

Abbott is seeking a Senior Director of Clinical Study Management to oversee a global portfolio of over 100 clinical studies within its Medical Devices division. The role requires a strategic leader with extensive experience in managing large-scale clinical trials and a strong understanding of global regulatory landscapes.

Salary

Base: $218,700.00 – $437,300.00; Bonus/Equity: Not specified; Benefits: Free medical coverage, retirement savings plan, tuition reimbursement

Skills & Requirements

Must-have

  • Leading large-scale pre-market clinical trials
  • Managing global studies and large budgets
  • Influencing study design for operational feasibility
  • Overseeing 400+ annual study milestones
  • Ensuring regulatory compliance across diverse areas

Nice-to-have

  • Experience in vascular or cardiovascular devices
  • Mentoring high-performing project management teams
  • Strategic partnership with business units
  • Continuous improvement mindset in operations

Key Requirements

  • Bachelor's degree in life sciences required
  • 7+ years experience leading pre-market clinical trials
  • Proven success managing global studies and large budgets
  • Advanced degree preferred
  • Strong leadership and cross-functional collaboration skills

Work Rights

Not specified

Tailored Resume

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