Global Study Lead - Remote Trials & Excellence

Parexel

Little Rock (AR)

Hybrid

USD 120,000 - 180,000

Full time

14 days+
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Job summary

Parexel is seeking a Global Study Manager II to provide operational leadership across the study lifecycle. You will oversee study management, site coordination, vendor deliverables, and cross-functional collaboration to ensure timely, high-quality data delivery.

The role requires extensive experience in study management, budget oversight, and vendor governance, with a focus on global regulatory readiness and continuous improvement.

Qualifications

  • Bachelor’s or higher degree in life sciences or related field.
  • Minimum 7 years of operational clinical trial experience (6 years if Master’s degree).
  • Experience with overseeing CROs and vendors.
  • GCP knowledge and regulatory operations familiarity.
  • Fluency in written and spoken English.

Responsibilities

  • Lead and coordinate global study execution from start-up to data release.
  • Provide oversight of regional operations and CRO tasks.
  • Set recruitment targets and delivery milestones for studies.
  • Develop and approve study startup, monitoring, and training plans.
  • Manage study budgets, vendor contracts, and per-subject costs.
  • Ensure TMF setup and inspection readiness.
  • Collaborate with CSTL and cross-functional teams.

Skills

Study management
Leadership
Budget management
Vendor management
Cross-functional collaboration
GCP knowledge
English fluency
Project planning
Risk management
Inspection readiness

Education

Bachelor’s degree in life sciences
Master’s degree in related field

Tools

CTMS
EDC
IRT

Job description

Parexel is seeking a Global Study Manager II to provide operational leadership across the study lifecycle. You will oversee study management, site coordination, vendor deliverables, and cross-functional collaboration to ensure timely, high-quality data delivery.

The role requires extensive experience in study management, budget oversight, and vendor governance, with a focus on global regulatory readiness and continuous improvement.

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