Global Clinical Operations Director – Study Management

Daiichi Sankyo, Inc.

Basking Ridge (NJ)

On-site

USD 263,000 - 439,000

Full time

5 days ago
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Job summary

The Executive Director, Global Clinical Operations Study Management Group Head at Daiichi Sankyo leads the study management portfolio across therapeutic areas, ensuring timely, high-quality, and cost-effective trial delivery. The role reports to the Global Clinical Operations VP and sets strategic direction for governance, standardization, and operational excellence.

You will partner with clinical development, regulatory, and data management teams, guide up to 10 staff, manage resources and

Qualifications

  • Bachelor's degree required in a related field.
  • 15+ years of industry experience in clinical operations.
  • Experience as Global Project Leader at Sr. Director level or equivalent preferred.
  • Proven global line management and staff development experience.
  • Strong strategic, innovative thinking and budgeting oversight.

Responsibilities

  • Provide leadership and strategic oversight of global clinical operations study management.
  • Ensure delivery of trials on time, quality, and within budget.
  • Partner with VP to develop functional standards and governance.
  • Collaborate with clinical development, regulatory, biostatistics, and data management.
  • Oversee budget planning and resource management across portfolio.
  • Escalate issues and maintain visibility with leadership.
  • Lead up to 10 direct reports and drive talent development.

Skills

Leadership
Communication
Budgeting
Cross-functional
Strategic thinking
People management
Change management
Global leadership

Education

Bachelor's Degree

Job description

The Executive Director, Global Clinical Operations Study Management Group Head at Daiichi Sankyo leads the study management portfolio across therapeutic areas, ensuring timely, high-quality, and cost-effective trial delivery. The role reports to the Global Clinical Operations VP and sets strategic direction for governance, standardization, and operational excellence.

You will partner with clinical development, regulatory, and data management teams, guide up to 10 staff, manage resources and

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