Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
ICON plc

Clinical Research Associate

ICON plc

Clinical Research Associate coordinating clinical trial monitoring and ensuring compliance with protocols at ICON. Delivering high-quality outcomes through collaboration and stakeholder management.

Posted 7/7/2026full-timeRemote • 🇲🇽 MexicoJuniorMid-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's protocols. Capable of developing strong relationships with stakeholders while maintaining accurate study documentation and reports.

Highest-signal resume keywords
Clinical Trial MonitoringICH-GCP GuidelinesStudy Documentation ManagementExcellent Communication SkillsStakeholder Relationship Management

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial CoordinationMedical Data EvaluationStudy Status ReportingFeasibility Study PreparationRegulatory Compliance
Soft Skills
Social SkillsTimely Query Resolution
Industry Keywords
Patient SafetyStudy Cost EfficiencyUniversity Degree in MedicineUniversity Degree in Science

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Deliver clinical trial monitoring work to a high standard
  • 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