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ICON plc

Clinical Research Associate I

ICON plc

. Coordinate all activities for setting up and monitoring a study .

Posted 10/27/2026full-timeRemote • Pennsylvania • United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in clinical trial monitoring, ensuring compliance with ICH-GCP guidelines and ICON procedures while maintaining accurate study documentation and fostering collaborative relationships with stakeholders. Proficient in evaluating medical data and communicating effectively in English.

Highest-signal resume keywords
Clinical Trial Monitoring ExperienceKnowledge Of ICH-GCP GuidelinesMedical Data EvaluationExcellent Written And Verbal CommunicationStudy Documentation Management

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
Study CoordinationStudy Status ReportingCost Efficiency ManagementFeasibility Study PreparationRegulatory Compliance
Soft Skills
Good Social SkillsTimely Query Resolution
Industry Keywords
Patient SafetyClinical InvestigatorsStakeholder CollaborationStudy DocumentationTravel Willingness

About the role

Key responsibilities & impact
  • Coordinate all activities for setting up and monitoring a study
  • Complete accurate study status reports and maintain study documentation
  • Run sponsor-generated queries efficiently
  • Take responsibility for study cost efficiency
  • Participate in preparing and reviewing study documentation and feasibility studies for new proposals
  • Develop and maintain collaborative relationships with key stakeholders, clinical investigators, and site staff
  • Ensure patient safety and compliance with ICON procedures, protocols, and regulatory requirements

Requirements

What you’ll need
  • University degree in medicine, science, or equivalent
  • Relevant clinical trial monitoring experience
  • Knowledge of ICH-GCP guidelines
  • Expertise to review and evaluate medical data
  • 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 (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