Clinical Trial Manager

ICON plc

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

Posted 9/18/2026full-timeRemote • North Carolina • 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, including planning, execution, and compliance with regulations. Proven ability to collaborate with cross-functional teams and manage relationships with stakeholders to ensure successful trial outcomes.

Highest-signal resume keywords

Clinical Trial ManagementPhase I Study ManagementRegulatory ComplianceStakeholder Relationship ManagementProblem-Solving

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial Protocol DevelopmentBudget ManagementTimeline AdherenceRisk ManagementVendor Selection

Soft Skills

CollaborationDecision-MakingCommunication

Industry Keywords

Clinical TrialsEthical GuidelinesInvestigatorsCross-Functional TeamsQuality Standards

About the role

Key responsibilities & impact

Manage day-to-day clinical trial management activities, supporting the team to deliver quality outcomes
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 to deliver high-quality outcomes across clinical programmes

Requirements

What you’ll need

University degree in medicine, science, or equivalent combination of education & experience
A minimum of three years of industry clinical trial management experience
Demonstrated ability to drive the clinical deliverables of a study
Experience managing phase I (healthy volunteer) studies
Some travel may be required
Employment with ICON is contingent upon having the 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