micro1Other AI work
Regulatory Affairs Specialist
up to $80/hr
About this role, in micro1's words
micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.
What you'll do
Scope of Work
- Author and review evaluation tasks inspired by real-world agency requests and sponsor response threads, determining if drafted responses meet regulatory expectations.
- Apply expert judgment to review clinical documentation, assessing whether conclusions are substantiated, commitments are properly scoped, and records can withstand regulatory scrutiny.
- Distinguish between substantively adequate and superficially polished responses, articulating clear rationales for any deficiencies.
Show all 6 itemsHide the other 3 in Scope of Work
- Assess consistency across comprehensive document sets, identifying unsupported or conflicting claims within or between documents.
- Provide structured, well-reasoned written feedback grounded in applicable regulatory guidelines rather than subjective impressions.
- Collaborate asynchronously and communicate complex regulatory concepts clearly in both written and verbal form.
Candidate background
Preferred Qualifications
- 5+ years of direct regulatory affairs experience at a sponsor, CRO, or consultancy, with responsibility for clinical submissions.
- Documented experience drafting or leading responses to health authority information requests, particularly for ongoing regulatory filings.
- Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada).
Show all 7 itemsHide the other 4 in Preferred Qualifications
- Proven ability to critically read clinical or safety documents to identify regulatory risks, unsupported statements, and potential reviewer concerns.
- Exceptional written communication skills, with the capability to convey regulatory reasoning clearly, concisely, and defensibly.
- Degree in life sciences, pharmacy, medicine, or a related field; RAC certification is an advantage.
- Experience engaging with multiple regions or agencies, prior health authority reviewer/assessor background, or familiarity with AI-assisted regulatory tools (all considered valuable).
Quoted from selected sections of micro1's posting. The full posting may state other conditions. Read the full posting
A closer look
More context, when you need it.
Full job descriptionThe original posting, in micro1's words
Posted by micro1, reproduced here so you can judge the role before clicking. Original posting ↗
Role Title: Regulatory Affairs Specialist
Role Type: Contractor
Location: Remote
micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.
Scope of Work
• Author and review evaluation tasks inspired by real-world agency requests and sponsor response threads, determining if drafted responses meet regulatory expectations.
• Apply expert judgment to review clinical documentation, assessing whether conclusions are substantiated, commitments are properly scoped, and records can withstand regulatory scrutiny.
• Distinguish between substantively adequate and superficially polished responses, articulating clear rationales for any deficiencies.
• Assess consistency across comprehensive document sets, identifying unsupported or conflicting claims within or between documents.
• Provide structured, well-reasoned written feedback grounded in applicable regulatory guidelines rather than subjective impressions.
• Collaborate asynchronously and communicate complex regulatory concepts clearly in both written and verbal form.
Preferred Qualifications
• 5+ years of direct regulatory affairs experience at a sponsor, CRO, or consultancy, with responsibility for clinical submissions.
• Documented experience drafting or leading responses to health authority information requests, particularly for ongoing regulatory filings.
• Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada).
• Proven ability to critically read clinical or safety documents to identify regulatory risks, unsupported statements, and potential reviewer concerns.
• Exceptional written communication skills, with the capability to convey regulatory reasoning clearly, concisely, and defensibly.
• Degree in life sciences, pharmacy, medicine, or a related field; RAC certification is an advantage.
• Experience engaging with multiple regions or agencies, prior health authority reviewer/assessor background, or familiarity with AI-assisted regulatory tools (all considered valuable).
Working with micro1Pay, getting started and work, from micro1's own pages
What the platform publishes in general. These are not extra terms confirmed for this particular role.
- Getting paid
- Paid in US dollars twice a month through Deel, usually landing around the 5th and the 20th. Nothing is paid until Deel's identity check is done. library.micro1.ai/working/faqs, library.micro1.ai/working/payroll-policy
- Before your first paid task
- An AI interview with micro1's recruiter Zara, then your profile, ID verification, a KarmaCheck background check and the Deel contract. Some pipelines add a quiz or test task. micro1.ai/experts, micro1.ai/ai-interview-guide, library.micro1.ai/getting-started/next-steps-after-certif..., library.micro1.ai/working/faqs, library.micro1.ai/working/what-to-expect
- How much work
- Certification makes you eligible but does not guarantee placement. micro1's FAQ puts the usual commitment at about 15 to 20 hours a week, depending on the client. micro1.ai/experts, library.micro1.ai/working/faqs
- Contract
- Independent contractor, with the contract issued through Deel. library.micro1.ai/policies/understanding-your-expert-agre..., library.micro1.ai/working/deel
Read on the pages linked above on 23 Sep 2026. Platforms change these terms, so check the linked page before you rely on one.
Alex's experience on micro1A personal account, not a promise about your project
Alexruns this site and has worked on micro1 himself. Written 31 Aug 2026.
- Every interview I took used an AI interviewer, and some included a timed business exercise of around 25 minutes.
- On later applications, interview reuse on micro1 was often partial, and I still answered questions about one to three additional skills.
- I entered a requested rate for the job. One listing showed about $180 an hour. I requested about $160 and received the rate I entered. Those amounts are approximate, and this describes my application, not proof that a lower request caused acceptance.
- Onboarding and setup came to about 2 hours, with clear materials. Of the three platforms I worked on, it was the easiest transition into work. That is an estimate from my projects, not a platform average.
- On my micro1 project, Hubstaff showed time and mouse or keyboard activity, not screenshots, app names or website history. That describes what I saw, not every possible setup.
- I was paid for hours logged, once every 14 days, and I have not experienced late or incorrect payments. That was my arrangement.
One person's applications, not a promise about yours.
What happens after you apply, first-handSources and listing historyWhere this information comes from
This listing's history
- First seen here on 24 Aug 2026, and still on micro1's list when we last read it on 13 Oct 2026.
- Listed pay changed on 5 Sep 2026: up to $70/hr before, up to $80/hr after.
A change can also be a correction to how we read micro1's feed. The figure at the top of this page is always the latest read.
- Posted by micro1
- First seen by AIPayList
- Last seen live
- Listing ID
- 7b914c4c-fe06-4b48-8337-320aca6681fb
Pay as the source states it: “micro1 job record, ideal_hourly_rate: $50–$80/hr”.
Platforms sometimes change a rate after posting. Every listing here is re-read at least once a day and corrected when its source moves, so a difference you see on the platform is usually a change made since the last read. How freshness works.
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