micro1Domain experts
Pharmacovigilance Expert
up to $80/hr
About this role, in micro1's words
micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. 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. This opportunity is ideal for professionals experienced in authoring and reviewing complex safety reports, passionate about data quality, and committed to clear written and verbal communication.
What you'll do
Scope of Work
- Author and review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level records.
- Apply expert judgment to assess the accuracy and adequacy of interval safety findings, signal evaluations, and benefit-risk conclusions in alignment with best practices.
- Assess template and structural conformity to ICH E2F and ICH E2C requirements, including proper section content, presentation of cumulative versus interval data, and completeness of appendices.
Show all 6 itemsHide the other 3 in Scope of Work
- Reconcile figures and case counts across report sections and data sources, identifying and documenting discrepancies significant for regulatory review.
- Evaluate safety conclusions in light of new data or events, and provide clear, structured written rationales supporting your determinations.
- Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis.
Candidate background
Preferred Qualifications
- 5+ years of pharmacovigilance or drug safety experience at a sponsor, CRO, or as an independent consultant.
- Demonstrated proficiency in authoring or reviewing DSURs and/or PSURs/PBRERs from start to finish.
- Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and benefit-risk assessment methodology.
Show all 7 itemsHide the other 4 in Preferred Qualifications
- Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness determination, and aggregate safety data analysis.
- Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level information.
- Advanced degree in life sciences, pharmacy, nursing, or medicine (PharmD, MD, MSc, or equivalent).
- Experience in both development-stage and post-marketing safety reporting, QPPV or deputy QPPV roles, safety committee participation, or AI-assisted safety review tools is a plus.
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: Pharmacovigilance Expert
Role Type: Contractor
Location: Remote
micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. 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. This opportunity is ideal for professionals experienced in authoring and reviewing complex safety reports, passionate about data quality, and committed to clear written and verbal communication.
Scope of Work
• Author and review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level records.
• Apply expert judgment to assess the accuracy and adequacy of interval safety findings, signal evaluations, and benefit-risk conclusions in alignment with best practices.
• Assess template and structural conformity to ICH E2F and ICH E2C requirements, including proper section content, presentation of cumulative versus interval data, and completeness of appendices.
• Reconcile figures and case counts across report sections and data sources, identifying and documenting discrepancies significant for regulatory review.
• Evaluate safety conclusions in light of new data or events, and provide clear, structured written rationales supporting your determinations.
• Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis.
Preferred Qualifications
• 5+ years of pharmacovigilance or drug safety experience at a sponsor, CRO, or as an independent consultant.
• Demonstrated proficiency in authoring or reviewing DSURs and/or PSURs/PBRERs from start to finish.
• Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and benefit-risk assessment methodology.
• Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness determination, and aggregate safety data analysis.
• Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level information.
• Advanced degree in life sciences, pharmacy, nursing, or medicine (PharmD, MD, MSc, or equivalent).
• Experience in both development-stage and post-marketing safety reporting, QPPV or deputy QPPV roles, safety committee participation, or AI-assisted safety review tools is a plus.
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-handHow does the pay compare?Across Domain experts roles, not this role alone
From our own daily reads of every open listing on the platforms we follow, not from micro1's posting. How we count.
Pay across the field: Domain experts
Across 698 roles in this field with a stated hourly rate in US dollars, on 18 platforms, the middle half pays $65 to $130 an hour at the top of the range, and the median is $100. This role's top rate, $80, is in the middle half. Of the 259 distinct rates we count, 97 are lower and 155 are higher.
| Platform | Roles | Top of range, per hour |
|---|---|---|
| Alignerr | 149 | $24 to $200 · median $80 |
| micro1 (this platform) | 135 | $28 to $400 · median $110 |
| AfterQuery | 88 | $45 to $175 · median $100 |
| Handshake AI | 79 | $30 to $300 · median $85 |
| Mercor | 78 | $55 to $450 · median $120 |
Sources 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.
- The listed pay has not changed since then.
- Posted by micro1
- First seen by AIPayList
- Last seen live
- Listing ID
- 176d0aa1-3dde-43d9-bb54-9f75f1c490dc
Pay as the source states it: “micro1 job record, ideal_hourly_rate: $70–$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.
Keep exploring
More like this
Related field, different requirements. Check each role's own page before you apply.