Global Study Manager

ICON plc

. Manage day-to-day clinical trial management activities .

Posted 11/3/2026full-timeRemote • CanadaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in clinical trial management, ensuring compliance with regulations and quality standards while effectively collaborating with cross-functional teams. Proven ability to manage competing priorities and drive clinical deliverables in a designated therapeutic area.

Highest-signal resume keywords

Clinical Trial ManagementRegulatory ComplianceCross-Functional CollaborationProblem-SolvingSubject Matter Expertise

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Trial Management ExperienceTrial Protocol DevelopmentRisk ManagementVendor SelectionMonitoring Experience

Soft Skills

Relationship BuildingDecision-MakingTeam Development

Industry Keywords

Clinical TrialsTherapeutic Area ExpertiseEthical GuidelinesLocal RegulationsNational RegulationsInternational Regulations

About the role

Key responsibilities & impact

Manage day-to-day clinical trial management activities
Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards
Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures
Build and manage strong relationships with trial investigators and stakeholders
Ensure trials comply with local, national, and international regulations and ethical guidelines
Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management
Support the team and stakeholders in delivering high-quality outcomes across clinical programmes

Requirements

What you’ll need

University degree in medicine, science, or equivalent combination of education & experience
Solid clinical trial management experience
Ability to manage competing priorities and develop your team
Demonstrated ability to drive the clinical deliverables of a study
Subject matter expertise in the designated therapeutic area
Prior monitoring experience is preferred
Willingness to travel as required (approximately 25%)
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