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ICON plc

Country Study Lead

ICON plc

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

Posted 11/5/2026full-timeRemote • Pennsylvania • United StatesSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing clinical trial activities, ensuring compliance with regulations and quality standards while collaborating effectively 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 CollaborationClinical DeliverablesTherapeutic 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 ProtocolsBudget ManagementRisk ManagementMonitoring ExperienceProblem-Solving
Soft Skills
Relationship ManagementDecision-MakingTeam Support
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 team members 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
  • 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