AI training contract
Medical Writer (Pharmaceutical)
Medicine & Health · USD 30-60 an hour. · 30 openings
Medical Writer (Pharmaceutical) 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 phd or academic credential, 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 30 to USD 60 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 30 openings on this role.
Skills named: regulatory medical writing, clinical study report authoring, ich e3 guidelines, scientific accuracy assessment, source data verification, clinical protocol interpretation, tfl (tables, figures, listings) analysis, written communication, structured feedback provision, collaborative problem-solving.
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: Medical Writer (Pharmaceutical) Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical 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 realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI. Preferred Qualifications Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued. Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.
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Rate, openings and requirements checked 2026-09-25 against micro1's own public postings.