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ICON plc

Global Study Manager

ICON plc

. Oversee clinical trial management workstreams, ensuring deliverables meet quality and timeline expectations .

Posted 11/6/2026full-timeRemote • United Kingdom, Romania, Poland, Hungary, BulgariaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical trial management, including protocol development, regulatory compliance, and data analysis. Proven ability to collaborate with cross-functional teams and effectively communicate with stakeholders to ensure successful trial execution.

Highest-signal resume keywords
Clinical Trial ManagementRegulatory ComplianceData AnalysisProtocol DevelopmentCross-Functional Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Trial DesignClinical Trial ExecutionData InterpretationAnalytical SkillsProblem-Solving Skills
Soft Skills
Effective CommunicationInterpersonal SkillsDetail-OrientedOrganizational SkillsAbility to Manage Competing Priorities
Industry Keywords
Clinical Trial ProtocolsRegulatory StandardsStakeholder CommunicationTrial EnrollmentStudy Outcomes Optimization

About the role

Key responsibilities & impact
  • Oversee clinical trial management workstreams, ensuring deliverables meet quality and timeline expectations
  • Collaborate with cross-functional teams to design and implement effective clinical trial enrollment
  • Develop and implement comprehensive clinical trial protocols with cross-functional teams
  • Oversee and manage day-to-day clinical trial operations, ensuring compliance with regulatory standards
  • Analyze and interpret clinical trial data, identify trends, and provide insights to optimize study outcomes
  • Proactively address challenges and implement effective solutions for successful clinical trial execution
  • Communicate with internal and external stakeholders to foster partnerships and facilitate smooth trial processes
  • Manage competing priorities and develop the team

Requirements

What you’ll need
  • Bachelor's degree in a relevant field
  • Ideally a minimum of 5 years of experience in clinical trial management
  • Proven expertise in designing and executing clinical trials
  • Strong understanding of regulatory requirements
  • Exceptional analytical and problem-solving skills
  • Ability to interpret complex medical data
  • Effective communication and interpersonal skills
  • Ability to collaborate across diverse teams
  • Detail-oriented and organized
  • Track record of successfully managing multiple tasks and priorities simultaneously
  • Legal right to work in the country where the role is based

Benefits

Comp & perks
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways