Regulatory Affairs Specialist (Pharma)
Paid in USD
Pharma & life sciences
New opportunity
Talent pool SpecialistContractRemote
Clinical Research Associate
Judge AI work on clinical trial conduct, monitoring and documentation.
At a glance
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Paid in USDHourly or per task, in USD. Your rate is agreed per project.
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Remote, any timezoneWork from anywhere with a stable connection.
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Flexible, part-timeChoose your own hours.
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Ongoing, project-based Starts when a matching project opens · Rolling applications
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Contract · SpecialistMultiple openings
About the work
Trial staff increasingly use AI to draft and check documents. Errors in this setting can harm patients or invalidate a study.
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 we are looking for
- 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
Hiring process
- Step 1Profile and CV review
- Step 2AI interview (about 20 minutes)
- Step 3Identity and credential check
- Step 4Short paid trial task
Free to apply. Vettedlance never charges candidates, and will never ask you to pay for training, tests or equipment.