Global Clinical Trial Operations Leader

Parexel

Boise (ID)

On-site

USD 100,000 - 150,000

Full time

5 days ago
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Job summary

Parexel is seeking a Clinical Trial Manager to drive execution of study-level activities, vendor oversight, and country/regional CRO operations across Phase I–IV trials. You will align feasibility, risk reviews, budgets, and timelines, and support training and onboarding of new team members.

The role emphasizes cross-functional leadership, strategic input on operational delivery, and collaboration with internal stakeholders to ensure successful study outcomes.

Qualifications

  • Minimum 5+ years of clinical research experience with a CRO/biotech/pharma on global Phase I–IV trials.
  • 2–3 years of experience leading aspects of global clinical trials.
  • Experience working with CROs.
  • Bachelor's degree is required.

Responsibilities

  • Manage integration of project team activities.
  • Oversee study operations including sites, regulatory submissions, drug supply, enrollment, budgets, and data flow.
  • Provide input on trial level operational strategies from protocol design to final study report.
  • Contribute to global subject/patient recruitment plans.
  • Oversee CRO/vendor identification and day-to-day management including SOWs and budgets.
  • Create and update critical trial documents.
  • Support training material development for compound and protocol levels.
  • Review budgets, timelines, and forecasts for studies.
  • Support inspection readiness with risk identification and mitigation.
  • Engage stakeholders and onboard new team members.
  • Attend meetings and provide updates on operational activities.

Skills

Decision making
Leadership
Matrixed/global environment
Mentoring
Organizational skills
Problem solving
Project planning/management
Study documentation
MS Office Suite
Travel readiness

Education

Bachelor's degree

Job description

Parexel is seeking a Clinical Trial Manager to drive execution of study-level activities, vendor oversight, and country/regional CRO operations across Phase I–IV trials. You will align feasibility, risk reviews, budgets, and timelines, and support training and onboarding of new team members.

The role emphasizes cross-functional leadership, strategic input on operational delivery, and collaboration with internal stakeholders to ensure successful study outcomes.

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