Global Clinical Trial Manager - Operations & CRO Leadership

Parexel

Frankfort (KY)

On-site

USD 110,000 - 160,000

Full time

10 days ago
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Job summary

Parexel in the United States is seeking a Clinical Trial Manager responsible for study-level delivery, including creation of trial documents, vendor oversight, and country/regional CRO management to ensure on-time, within-budget execution.

You will collaborate with cross-functional teams, oversee budgets, timelines, and risk reviews, contribute to feasibility and recruitment plans, and support inspection readiness and training materials.

Qualifications

  • Bachelor's degree required in a relevant field.
  • 5+ years of clinical research experience with CRO/biotech/pharma.
  • Experience with protocol, ICF, CRF, CSR development and review.
  • Experience interacting with CROs and global teams.

Responsibilities

  • Manage integration of project team activities across sites and vendors.
  • Oversee study operations including regulatory submissions, drug supply, enrollment, timelines, budget, metrics, and data flow.
  • Provide input on trial-level operational strategies from protocol design to final study report.
  • Contribute to global recruitment plans and site/vendor oversight.
  • Create and update trial-specific documents and training materials.
  • Support budgeting, timelines, forecasts, and inspection-readiness activities.
  • Interface with stakeholders and mentor new team members.

Skills

Decision making
Leadership
Cross-functional collaboration
Mentoring
Organizational skills
Problem solving
Project management
Communication
Protocol/CSR knowledge
MS Office
Travel readiness

Education

Bachelor's degree

Tools

MS Office Suite

Job description

Parexel in the United States is seeking a Clinical Trial Manager responsible for study-level delivery, including creation of trial documents, vendor oversight, and country/regional CRO management to ensure on-time, within-budget execution.

You will collaborate with cross-functional teams, oversee budgets, timelines, and risk reviews, contribute to feasibility and recruitment plans, and support inspection readiness and training materials.

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