Pharmacovigilance Specialist

At a glance

• Rate agreed per projectPaid weekly in USD
• Hourly or per-task contractIndependent contractor · Expert
• 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

Evaluate AI on adverse event reporting, case processing and drug safety signals.

Key responsibilities

• 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

Ideal qualifications

• 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 pharmacovigilance safety databases

More about the opportunity

Automated case intake is spreading fast in drug safety. Human experts define what a correct, complete case looks like.

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.