Clinical Research Associate

At a glance

• Rate agreed per projectPaid weekly in USD
• Hourly or per-task contractIndependent contractor · Specialist
• RemoteWork from anywhere with a stable connection.
• Flexible, part-timeChoose your own hours.
• Ongoing, project-based Starts when a matching project opens · Rolling applications

Role overview

Judge AI work on clinical trial conduct, monitoring and documentation.

Key responsibilities

• 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

Ideal qualifications

• Experience as a CRA or clinical trial coordinator
• Sound knowledge of ICH-GCP
• Professional written English
• Scientific or health degree

Nice to have

• Experience with trials in South Asia or the Middle East
• Knowledge of electronic data capture systems

More about the opportunity

Trial staff increasingly use AI to draft and check documents. Errors in this setting can harm patients or invalidate a study.

Compensation and contract terms

• Hourly or per task, in USD. Your rate is agreed per project.
• Hourly or per-task contract. You are engaged as an independent contractor.
• Remote. Flexible, part-time, on your own schedule.
• Paid weekly in USD for approved work.
• Projects can be extended, shortened or ended early depending on project needs and quality.

Application process

1. ApplyCreate a free profile and upload your CV.
2. InterviewAbout 20 minutes. You need a laptop or desktop with a camera and microphone.
3. ID and credential checkWe verify your identity and the qualifications the role needs.
4. Matched to projectsOnce verified, you are invited to paid projects that fit your skills.

Free to apply. Vettedlance never charges candidates, and will never ask you to pay for training, tests or equipment.