Clinical Research Associate

ICON plc

. Perform site qualification, initiation, monitoring and closeout activities as assigned .

Posted 11/12/2026full-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 processes, ICH Good Clinical Practice (GCP) guidelines, and regulatory compliance, with a strong focus on site qualification, monitoring, and closeout activities. Proven ability to communicate effectively with investigators and site staff while managing risks and ensuring participant protection.

Highest-signal resume keywords

Clinical Trial ProcessesICH Good Clinical Practice (GCP)Site MonitoringClinical Trial Management Systems (CTMS)Electronic Data Capture (EDC)

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Site QualificationMonitoring ActivitiesRegulatory ComplianceProtocol VerificationRisk Based MonitoringCentralised MonitoringParticipant ProtectionSite ManagementClinical Research ExperienceTherapeutic Area Expertise

Soft Skills

Clear CommunicationProblem Solving

Tools & Technologies

Clinical Trial Management Systems (CTMS)Electronic Data Capture (EDC)Electronic Trial Master File Systems

Industry Keywords

Life SciencesHealthcareClinical ResearchGood Clinical Practice (GCP)Regulatory Compliance

About the role

Key responsibilities & impact

Perform site qualification, initiation, monitoring and closeout activities as assigned
Contribute to clinical trial monitoring activities and take responsibility for deliverables
Verify protocol, GCP and regulatory compliance and participant protection
Review source data, essential documents and site processes for accuracy and completeness
Identify and follow up findings, risks and corrective actions
Maintain clear communication with investigators, site staff and study teams

Requirements

What you’ll need

Relevant life sciences, healthcare or clinical research qualification, or equivalent relevant clinical research experience
Minimum of 2 years of experience as a Clinical Research Associate
In-depth knowledge of clinical trial processes, regulations, and ICH Good Clinical Practice (GCP) guidelines
Knowledge of ICH Good Clinical Practice (GCP), clinical trial conduct and site monitoring requirements
Practical experience with site monitoring or site management appropriate to the level of role
Experience performing site qualification, initiation, monitoring and closeout activities as assigned
Experience verifying protocol, GCP and regulatory compliance and participant protection
Willingness to travel as required (approximately 60%)
Legal right to work in Mexico
Therapeutic area expertise relevant to assigned studies
Experience with risk based monitoring or centralised monitoring approaches
Experience with clinical trial management systems (CTMS), electronic data capture (EDC) and electronic trial master file systems

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