Remote Clinical Research Associate II — Global Trials
ICON Clinical Research
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Benefits offered by this job
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
Education
Tools
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.
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