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ICON plc

Clinical Research Associate 1

ICON plc

CRA I at ICON contributing to clinical trial operations function and collaborating to deliver high-quality outcomes. Working independently for study setup and monitoring while ensuring compliance with regulations.

Posted 6/18/2026full-timeRemote • 🇧🇷 BrazilJuniorMid-LevelWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Deliver clinical trial monitoring work to a high standard
  • Work closely with your team and stakeholders
  • Coordinate all activities for setting up and monitoring a study
  • Complete accurate study status reports and maintain study documentation
  • Run sponsor generated queries efficiently and take responsibility for study cost efficiency
  • Participate in the preparation and review of study documentation and feasibility studies for new proposals as required
  • Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
  • Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements

Requirements

What you’ll need
  • University degree in medicine, science, or equivalent
  • Knowledge of ICH-GCP guidelines and the 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%)

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

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Hard Skills & Tools
clinical trial monitoringstudy documentationstudy status reportsmedical data evaluationfeasibility studiesregulatory compliance
Soft Skills
communicationcollaborationrelationship buildingproblem-solvingtime management
Certifications
university degree in medicineuniversity degree in science