Lead Clinical Research Associate

ICON plc

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

Posted 9/30/2026full-timeRemote • United States, CanadaSeniorWebsite

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 and stakeholders. Proven ability to drive clinical deliverables and manage competing priorities in a dynamic environment.

Highest-signal resume keywords

Clinical Trial ManagementRegulatory ComplianceCross-Functional CollaborationTherapeutic Area ExpertiseProblem-Solving

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementTrial Protocol DevelopmentBudget ManagementRisk ManagementMonitoring Experience

Soft Skills

Relationship ManagementDecision-MakingTeam Development

Industry Keywords

Clinical TrialsEthical GuidelinesLocal RegulationsNational RegulationsInternational Regulations

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 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 development of the team and manage competing priorities

Requirements

What you’ll need

University degree in medicine, science, or equivalent combination of education & experience
Solid clinical trial management experience
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