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ICON plc

Clinical Research Associate – Level 1

ICON plc

. Deliver clinical trial monitoring work to a high standard .

Posted 10/15/2026full-timeRemote • United KingdomJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in clinical trial monitoring and in vitro diagnostics, ensuring compliance with FDA regulations and good clinical practice. Strong communication skills facilitate effective collaboration with stakeholders and timely resolution of queries.

Highest-signal resume keywords
Clinical Trial MonitoringIn Vitro DiagnosticsGood Clinical Practice (GCP)Regulatory SubmissionsFederal Regulations

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical ResearchStudy ProtocolsData ValidationSOP ImplementationStudy Coordination
Soft Skills
Excellent CommunicationSocial SkillsTeam Collaboration
Industry Keywords
FDA RegulationsIVD DirectivesClinical Trial ProcessesLaboratory BackgroundUniversity Degree in Medicine or Science

About the role

Key responsibilities & impact
  • Deliver clinical trial monitoring work to a high standard
  • Work closely with the team and stakeholders
  • Ensure studies are conducted according to study protocols, operating procedures, and good clinical practice
  • Validate product performance claims
  • Supply data for critical Regulatory submissions
  • Define the functional and clinical utility of investigation products
  • Understand and implement federal regulations
  • Help roll out SOPs to ensure studies adhere to FDA regulations, GCP, IVD directives, and client policy
  • Contribute to designing, planning, coordinating, and conducting activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics

Requirements

What you’ll need
  • University degree in medicine, science, or equivalent
  • Practical knowledge of in vitro diagnostics and clinical trial processes
  • Excellent written and verbal communication in English
  • Good social skills enabling you to deal with queries in a timely manner
  • Willingness to travel as required from your UK base (occasionally internationally)
  • Relevant In Vitro Diagnostics experience, ideally from a laboratory background
  • 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