Regulatory Affairs Specialist (Pharma)

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 answers on drug registration, submissions and regulatory requirements across markets.

Key responsibilities

• 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• Flag outdated or wrong guidance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

Ideal qualifications

• 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

More about the opportunity

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.

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.