AI training contract
Pharmacovigilance Expert
Medicine & Health · USD 70-80 an hour. · 40 openings
Pharmacovigilance Expert is contract work for micro1, reviewing and correcting what AI models produce in medicine & health. The output of the job is expert judgement written down: a model gives an answer, someone who knows the subject decides whether it is right and explains why.
What it requires. This role is gated on medical licence. Applications without it are not considered, and the requirement is stated here because the original advert usually carries it well below the rate.
What it pays. USD 70 to USD 80 an hour, as published by micro1. Rates in this category track how rare the credential is rather than how hard the work is.
Where. The listing says this role is remote and names no country. micro1 says it hires talent from around the world, except people who reside in Afghanistan, Belarus, China, Cuba, Democratic Republic of the Congo, Hong Kong, Iran, Iraq, Libya, Macao, Myanmar, North Korea, Russian Federation, Somalia, South Sudan, Sudan, Syria, Venezuela, Ukraine, and Yemen. So this page lists every other country as eligible, on the strength of that rule and not of anything this listing says. Requirements can still differ by role, so check the application page on micro1 before you apply.
micro1 lists 40 openings on this role.
Skills named: pharmacovigilance, drug safety report authoring, dsur/psur/pbrer review, ich e2f and ich e2c(r2) compliance, gvp guidelines, aggregate safety data analysis, signal management, benefit-risk assessment, meddra coding, seriousness and causality assessment.
Applications are made on micro1, not here. WFA Digital is independent of micro1 and may receive a referral fee if you are hired, at no cost to you.
Full listing, as published by micro1
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.
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Rate, openings and requirements checked 2026-09-25 against micro1's own public postings.