Regulatory Affairs Specialist (Pharma)
Paid in USD
Pharma & life sciences
New opportunity
Talent pool ExpertContractRemote
Pharmacovigilance Specialist
Evaluate AI on adverse event reporting, case processing and drug safety signals.
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
Automated case intake is spreading fast in drug safety. Human experts define what a correct, complete case looks like.
What you will do
- Check model case narratives and seriousness assessments
- Test coding of adverse events with MedDRA
- Write safety scenarios with correct handling
- Flag answers that could delay or miss a safety report
What we are looking for
- Pharmacovigilance or drug safety experience
- Knowledge of ICH E2 guidelines and reporting timelines
- Pharmacy, medicine or life science degree
- Professional written English
Nice to have
- Signal detection or aggregate report experience
- Familiarity with safety databases such as Argus
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.