Associate Director Regional Clinical Operations

ICON Clinical Research, LP

Multiple Locations
Oversight of assigned studies
Country study goals and commitments
Relationships with key institutions
Accountable for oversight of all assigned studies within the country in accordance with the overall development plan and clinical operations plan and under the direction of the global team (Global Clinical Trial Manager), including adherence to quality, timelines and budget

Job Summary

  • Accountable for oversight of all assigned studies within the country in accordance with the overall development plan and clinical operations plan and under the direction of the global team (Global Clinical Trial Manager), including adherence to quality, timelines and budget.
  • Drive the identification and inclusion of sites that have access to and can enroll patients who are from groups that have been historically underrepresented in clinical trials (per FDA Guidance for Industry for Improving Enrollment of Participants from Underrepresented Racial and Ethnic Populations in Clinical Trials).
  • Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Matching Summary

Accountable for oversight of all assigned studies within the country in accordance with the overall development plan and clinical operations plan and under the direction of the global team (Global Clinical Trial Manager), including adherence to quality, timelines and budget.

Skills & Requirements

Must-have

  • Oversight of assigned studies
  • Country study goals and commitments
  • Relationships with key institutions
  • Site monitoring performance
  • Evidence-based site recommendations
  • Cross-functional collaboration

Nice-to-have

  • Fostering inclusive environment
  • Driving innovation and excellence
  • Shaping the future of clinical development
  • Work-life balance opportunities

Key Requirements

  • Bachelor’s degree with 5-7 years experience
  • Minimum 3 years primary responsibility for clinical trial execution
  • Direct management experience and supervisory responsibility
  • Travel up to 20% (domestic and international)

Work Rights

Not specified

Tailored Resume

Cover Letter