Home-Based CRA II: Clinical Trial Monitoring

ICON plc

Estado de México

Hybrid

MXN 420,000 - 660,000

Full time

2 days ago
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Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II to support site qualification, initiation, monitoring and closeout activities, primarily on sponsor-dedicated trials. This remote role is based in Mexico, with occasional travel as needed.

You will verify protocol, GCP and regulatory compliance, review source data and essential documents, and maintain timely communication with investigators and study teams. A life sciences qualification and 2+ years CRA experience are required.

Qualifications

  • Relevant life sciences, healthcare or clinical research qualification.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH GCP guidelines.
  • Knowledge of ICH GCP, trial conduct and site monitoring requirements.
  • Experience with site monitoring or site management relevant to the role.

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

GCP knowledge
Site monitoring
Regulatory compliance
Investigator communication

Education

Life sciences qualification

Tools

CTMS
EDC
eTMF

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II to support site qualification, initiation, monitoring and closeout activities, primarily on sponsor-dedicated trials. This remote role is based in Mexico, with occasional travel as needed.

You will verify protocol, GCP and regulatory compliance, review source data and essential documents, and maintain timely communication with investigators and study teams. A life sciences qualification and 2+ years CRA experience are required.

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