Global Clinical Study Manager | Lead Trials & Compliance

ICON Strategic Solutions

United Kingdom

On-site

GBP 60,000 - 75,000

Full time

41 hours ago
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Benefits offered by this job

Annual leave entitlements
Health insurance offerings
Competitive retirement planning
Global Employee Assistance Programme (
Life assurance
Country-specific benefits including (e

Job summary

ICON Strategic Solutions is seeking a Global Study Manager to oversee day-to-day clinical trial management, ensure timely delivery, and support cross-functional teams. The role emphasizes regulatory compliance, quality outcomes, and stakeholder collaboration.

The position requires a medical or scientific degree with trial management experience and a willingness to travel up to 25%. You will lead study delivery within a sponsor-dedicated model and contribute to patient-centered therapeutic

Qualifications

  • University degree in medicine, science, or equivalent combination of education & experience.
  • Ability to drive the clinical deliverables of a study.
  • Subject matter expertise in the designated therapeutic area.
  • Willingness to travel as required (approximately 25%)

Responsibilities

  • Plan and manage day-to-day clinical trial management activities, delivering quality outcomes.
  • Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
  • Build and manage relationships with trial investigators and stakeholders.
  • Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
  • Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Skills

Clinical trial management

Education

University degree in medicine, science, or equivalent combination of education & experience

Job description

ICON Strategic Solutions is seeking a Global Study Manager to oversee day-to-day clinical trial management, ensure timely delivery, and support cross-functional teams. The role emphasizes regulatory compliance, quality outcomes, and stakeholder collaboration.

The position requires a medical or scientific degree with trial management experience and a willingness to travel up to 25%. You will lead study delivery within a sponsor-dedicated model and contribute to patient-centered therapeutic

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