ICON plc

Clinical Associate

ICON plc
Posted 10/21/2026full-timeRemote • MexicoJuniorMid-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 clinical trial coordination, ensuring adherence to regulatory guidelines and protocol requirements while maintaining data accuracy and compliance. Strong collaboration skills with cross-functional teams to support successful clinical study execution.

Highest-signal resume keywords
Clinical Trial CoordinationRegulatory ComplianceData Collection and DocumentationCross-Functional CollaborationOrganizational and Time Management Skills

About the role

Key responsibilities & impact
  • Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards
  • Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely and accurate data collection and documentation
  • Collaborate with cross-functional teams including Clinical Operations, Data Management, and Biometrics to support the successful execution of clinical trials
  • Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations and standard operating procedures
  • Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports
  • Take responsibility for clinical coordination deliverables and work collaboratively

Requirements

What you’ll need
  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry
  • Strong organizational and time management skills, with the ability to prioritize tasks and manage competing priorities effectively
  • Excellent attention to detail and problem-solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance
  • Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and build strong relationships with study teams and clinical sites
  • 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 ResearchData AnalysisStudy DocumentationProtocol AdherencePatient Recruitment
Soft Skills
Attention to DetailProblem-Solving AbilitiesEffective CommunicationInterpersonal Skills
Industry Keywords
Pharmaceutical IndustryBiotechnologyCRO IndustryClinical OperationsBiometrics