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ICON plc

Clinical Trial Manager

ICON plc

. Manage day-to-day clinical trial management activities .

Posted 10/16/2026full-timeRemote • BrazilMid-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. Proven ability to drive clinical deliverables and manage relationships with stakeholders in the therapeutic area.

Highest-signal resume keywords
Clinical Trial ManagementRegulatory ComplianceStakeholder Relationship ManagementProblem-SolvingTherapeutic Area Expertise

ATS Keywords

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Applicant Tracking System Keywords

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

Hard Skills
Clinical Trial ManagementClinical DeliverablesTrial Protocol DevelopmentRisk ManagementVendor SelectionMonitoring Experience
Soft Skills
CollaborationDecision-MakingCommunication
Industry Keywords
Clinical TrialsEthical GuidelinesLocal RegulationsNational RegulationsInternational Regulations

About the role

Key responsibilities & impact
  • Manage day-to-day clinical trial management activities
  • 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 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
  • 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