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ICON plc

Clinical Research Associate

ICON plc

. Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials .

Posted 9/21/2026full-timeRemote • United StatesJuniorMid-Level💰 $91,336 - $114,170 per yearWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in clinical trial processes, including site qualification, monitoring, and compliance with ICH-GCP guidelines. Strong ability to ensure data integrity and patient safety while collaborating effectively with investigators and site staff.

Highest-signal resume keywords
Clinical Trial ProcessesOncology Monitoring ExperienceICH-GCP GuidelinesData IntegrityStudy Documentation Preparation

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Research Associate ExperienceProtocol ComplianceData ReviewQuery ResolutionStudy Documentation Review
Soft Skills
Strong Organizational SkillsCommunication SkillsAttention to DetailAbility to Work IndependentlyCollaborative Skills
Industry Keywords
Clinical TrialsPatient SafetyScientific DegreeHealthcare-Related FieldTravel Willingness

About the role

Key responsibilities & impact
  • 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 resolution of 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
  • Oncology monitoring experience required
  • 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 up to 60%-75% within their region
  • Legal right to work in the country where the role is based

Benefits

Comp & perks
  • Competitive base salary and performance related incentives
  • 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