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Clinical Research Associate

Vettedlance

Judge AI work on clinical trial conduct, monitoring and documentation. What you will do Review model answers on trial protocols, monitoring and GCP Write scenarios on consent, deviations and source data checks Check AI-drafted trial documents for errors Rate answers for accuracy and safety What you need Experience as a CRA or clinical trial coordinator Sound knowledge of ICH-GCP Professional written English Scientific or health degree Contract Remote, hourly or per-task contract (independent contractor) Part-time, flexible: 10–40 hrs/week Remote Hourly or per task, in USD. Your rate is agreed per project. #J-18808-Ljbffr Vettedlance

Vacancy posted 1 day ago
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