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ICON plc

Clinical Research Associate II

ICON plc

. Design and analyse clinical trials, interpreting complex medical data .

Posted 10/8/2026full-timeRemote • ChinaJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in clinical trial design, monitoring, and compliance with ICH-GCP guidelines, ensuring data integrity and patient safety. Strong organizational and communication skills facilitate effective collaboration with investigators and site staff.

Highest-signal resume keywords
Clinical Trial DesignICH-GCP GuidelinesClinical Trial MonitoringData IntegrityCommunication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Trial ProcessesData ReviewProtocol ComplianceSite QualificationSite InitiationMonitoring VisitsClose-Out VisitsStudy Documentation PreparationMedical Data InterpretationQuery Resolution
Soft Skills
Organizational SkillsAttention to DetailIndependent WorkCollaborative WorkFast-Paced Environment Adaptability
Industry Keywords
Clinical Research AssociateHealthcare FieldPatient SafetyStudy ReportsTravel Requirement

About the role

Key responsibilities & impact
  • Design and analyse clinical trials, interpreting complex medical data
  • Contribute to clinical trial monitoring activities and take responsibility for deliverables
  • Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensure protocol compliance, data integrity, and patient safety throughout the trial process
  • Collaborate with investigators and site staff to facilitate smooth study conduct
  • Perform data review and resolve queries to maintain high-quality clinical data
  • Contribute to the preparation and review of study documentation, including protocols and clinical study reports

Requirements

What you’ll need
  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 2 years of experience as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills, with attention to detail
  • Ability to work independently and collaboratively in a fast-paced environment
  • Willingness to travel as required (approximately 60%)
  • Employment with ICON is contingent upon having the 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