Clinical Research Associate
Paid in USD
Pharma & life sciences
New opportunity
Talent pool ExpertContractRemote
Regulatory Affairs Specialist (Pharma)
Evaluate AI answers on drug registration, submissions and regulatory requirements across markets.
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 · ExpertMultiple openings
About the work
Regulatory rules change often and differ by country. AI tools used in this field must be checked by people who file submissions for a living.
What you will do
- Check model answers on dossiers, variations and approval pathways
- Write realistic regulatory questions with model answers
- Flag outdated or wrong guidance
- Compare requirements across regulators
What we are looking for
- Professional regulatory affairs experience in pharma, biologics or devices
- Working knowledge of CTD format and major regulators
- Professional written English
- Attention to detail
Nice to have
- Experience with DRAP, SFDA, EMA or FDA submissions
- RAC or similar certification
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.