Clinical Trial Manager

ICON plc

Clinical Trial Manager at ICON managing clinical trial operations and ensuring high-quality outcomes. Collaborating with stakeholders and adhering to timelines, budget, and regulations.

Posted 7/14/2026full-timeRemote • 🇬🇷 GreeceMid-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 and stakeholders. Proven ability to drive clinical deliverables and make critical decisions in trial design and risk management.

Highest-signal resume keywords

Clinical Trial ManagementRegulatory ComplianceCross-Functional CollaborationProblem-SolvingSubject Matter Expertise

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

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

Hard Skills

Clinical Trial ProtocolsBudget ManagementTimeline AdherenceVendor SelectionRisk Management

Soft Skills

Relationship BuildingDecision-Making

Industry Keywords

Clinical TrialsTherapeutic Area ExpertiseMonitoring ExperienceEthical GuidelinesLocal and National Regulations

About the role

Key responsibilities & impact

Manage day-to-day clinical trial management activities, supporting your 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 all trials are conducted in compliance with local, national, and international regulations and ethical guidelines
Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management

Requirements

What you’ll need

University degree in medicine, science, or equivalent combination of education & 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%)

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