ICON plc

Clinical Research Associate – 3

ICON plc
Posted 10/22/2026full-timeRemote • AustraliaJuniorMid-LevelWebsite
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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 adherence to protocols and regulatory requirements while fostering collaboration across teams. Proficient in monitoring practices, data integrity, and site management to drive compliance and successful trial execution.

Highest-signal resume keywords
Clinical Trial ManagementGood Clinical Practice (GCP)Site MonitoringData IntegrityStakeholder Management

About the role

Key responsibilities & impact
  • Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards
  • Lead clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement
  • Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
  • Conduct site visits to assess site performance, resolve issues, and support successful trial execution
  • Collaborate with cross-functional teams on timely and accurate data collection and reporting
  • Provide training and guidance to site staff and other CRAs
  • Build and maintain relationships with site personnel and stakeholders to facilitate smooth trial operations

Requirements

What you’ll need
  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
  • Proven ability to manage multiple sites and projects simultaneously
  • Strong organizational and problem-solving skills
  • Expertise in monitoring practices, data integrity, and site management
  • Proficiency in relevant clinical trial software and tools
  • Excellent communication, interpersonal, and stakeholder management skills
  • Ability to influence and drive compliance within a complex environment
  • Willingness to travel as required (approximately 60%)
  • 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

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 ProcessesRegulatory RequirementsSite ManagementMonitoring PracticesData CollectionProblem-SolvingOrganizational Skills
Soft Skills
Communication SkillsInterpersonal SkillsInfluencing Skills
Tools & Technologies
Clinical Trial Software
Industry Keywords
Clinical Research AssociateTrial ExecutionCross-Functional CollaborationSite Performance Assessment