Remote CRA II – Clinical Monitoring & Site Qualification

ICON Clinical Research; Estado de México; Hybrid; MXN 350,000 - 700,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee Assistance Programme

Life assurance

Flexible benefits

Job summary

ICON Strategic Solutions in Mexico is seeking a CRA II for a home-based role. You will conduct site qualification, initiation, monitoring and closeout activities, ensuring compliance with protocol, GCP and regulatory requirements.

You'll review source data and essential documents, identify risks, and communicate with investigators and study teams. Travel up to 60% is expected to support sponsor-led trials.

Qualifications

• Relevant life sciences, healthcare or clinical research qualification, or equivalent.
• Minimum 2 years of experience as a Clinical Research Associate.
• Strong knowledge of clinical trial processes, regulations and ICH GCP.
• Knowledge of GCP, trial conduct and site monitoring requirements.
• Experience with site monitoring or site management.
• Experience performing site qualification, initiation, monitoring and closeout.
• Experience verifying protocol, GCP and regulatory compliance.

Responsibilities

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

Skills

Site Monitoring

CRA Experience

GCP Knowledge

Regulatory Compliance

Communication

Clinical Trial Processes

Education

Life sciences / clinical research qualification

Tools

CTMS

EDC

eTMF

Job description

ICON Strategic Solutions in Mexico is seeking a CRA II for a home-based role. You will conduct site qualification, initiation, monitoring and closeout activities, ensuring compliance with protocol, GCP and regulatory requirements.

You'll review source data and essential documents, identify risks, and communicate with investigators and study teams. Travel up to 60% is expected to support sponsor-led trials.