Global Study Manager

ICON plc

. Coordinate clinical trial management delivery, resolve issues, and develop team capability .

Posted 11/4/2026full-timeRemote • Canada, United StatesMid-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 regulatory requirements while effectively coordinating resources, budgets, and timelines. Strong focus on data integrity and quality assurance throughout the study lifecycle.

Highest-signal resume keywords

Clinical Study ManagementProject Management SkillsRegulatory ComplianceData IntegrityInterpersonal Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementBudget ManagementStudy ExecutionMonitoring ProcessesData Validation

Soft Skills

CollaborationDetail-OrientedProblem ResolutionPrioritizationCommunication Skills

Industry Keywords

Drug Development ProcessRegulatory RequirementsClinical StudiesStakeholder CollaborationQuality Standards

About the role

Key responsibilities & impact

Coordinate clinical trial management delivery, resolve issues, and develop team capability
Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines
Collaborate with investigators, vendors, and internal stakeholders to implement clinical studies successfully
Develop and manage study budgets, resources, and timelines
Lead resolution of issues and challenges arising during clinical trials
Ensure data integrity and quality through monitoring and validation processes throughout the study lifecycle

Requirements

What you’ll need

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Proven experience in clinical study management, with a strong understanding of the drug development process and regulatory requirements
Excellent project management skills, including the ability to handle multiple tasks simultaneously and prioritize effectively
Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners
Detail-oriented with a focus on ensuring data accuracy and maintaining high-quality standards in clinical trials
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