Manager, Clinical Trial Management

ICON plc

. Manage day-to-day clinical trial management activities, supporting the team to deliver quality outcomes .

Posted 10/30/2026full-timeRemote • ChinaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial management, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP). Proven ability to lead cross-functional teams, manage project timelines and budgets, and mitigate risks effectively.

Highest-signal resume keywords

Clinical Trial ManagementRegulatory ComplianceGood Clinical Practice (GCP)Leadership SkillsAnalytical Problem-Solving

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementRegulatory ComplianceGood Clinical Practice (GCP)Project ManagementRisk MitigationStudy PlanningBudget ManagementOperational OversightTrial Close-OutCross-Functional Collaboration

Soft Skills

Leadership SkillsCommunication SkillsMotivational SkillsAnalytical SkillsProblem-Solving Skills

Industry Keywords

Clinical ResearchLife SciencesTrial ManagementComplianceStudy Initiation

About the role

Key responsibilities & impact

Manage day-to-day clinical trial management activities, supporting the team to deliver quality outcomes
Manage the overall operational aspects of clinical trial projects, from study initiation through to close-out
Collaborate with cross-functional teams to develop study plans, timelines, and budgets, ensuring alignment with project goals
Oversee the performance of Clinical Trial Managers and study teams, providing guidance and support as needed
Ensure compliance with regulatory requirements, Good Clinical Practice (GCP), and internal policies throughout the trial process
Identify risks and implement strategies to mitigate them, ensuring the successful delivery of clinical trials

Requirements

What you’ll need

Degree in life sciences, clinical research, or a related field
Significant experience in clinical trial management, with a proven track record of leading successful trials
Strong understanding of regulatory requirements and GCP in clinical research
Excellent leadership and communication skills, with the ability to motivate and manage cross-functional teams
Proven analytical and problem-solving skills, capable of navigating complex project challenges
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