AI training contract
Clinical Publications Author
Science & Research · USD 50-80 an hour. · 50 openings
Clinical Publications Author is contract work for micro1, reviewing and correcting what AI models produce in science & research. 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 50 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 50 openings on this role.
Skills named: medical writing, scientific publication authoring, peer-reviewed manuscript preparation, publication guidelines (icmje, gpp3/gpp2022, consort), journal submission workflows, clinical data interpretation, data verification, structured feedback writing, publication ethics (equator network, strobe), advanced written communication.
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: Clinical Publications Author Role Type: Contractor Location: Remote micro1 is engaging Clinical Publications Authors to participate in a customer’s project focused on developing advanced AI-assisted tools for medical and scientific writing. 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 Task Authoring & Review: Author and review realistic evaluation tasks based on peer-reviewed journal manuscripts, scientific abstracts, conference posters, and presentation decks to inform AI tool development. Structural & Formatting Assessment: Apply expert judgment to assess whether AI-generated draft sections align with publisher formatting standards, journal guidelines, and international publication ethics (such as ICMJE, GPP, and relevant EQUATOR Network reporting guidelines like CONSORT or STROBE). Scientific Accuracy & Interpretation: Evaluate scientific accuracy in manuscripts, abstracts, and discussion sections, distinguishing true errors in data interpretation or medical reasoning from stylistic or editorial preferences. Data Verification: Trace publication claims and narratives directly to source records—such as Clinical Study Reports (CSRs), protocols, and Tables, Figures, and Listings (TFLs)—to verify that all statements are accurately grounded in data. Structured Feedback: Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior. Framework Refinement: Collaborate with project leads to refine evaluation criteria and document best practices for scientific publishing workflows within AI development environments. Preferred Qualifications Minimum 5 years of dedicated medical/scientific publication authoring experience within a sponsor, CRO, MedComms agency, or as an independent consultant. Direct experience lead-authoring or managing peer-reviewed manuscripts published in reputable biomedical or clinical journals. Strong working knowledge of publication guidelines (ICMJE, GPP3/GPP2022, CONSORT), copyright compliance, and journal submission workflows. Demonstrated capability to interpret complex clinical data (TFLs, statistical analysis plans) and translate them into clear, publication-ready scientific narratives. Exceptional written communication skills, with a proven track record of providing actionable, structured feedback on scientific draft materials. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc) or equivalent depth of authoring experience. Therapeutic area diversity across multiple clinical phases; expertise in oncology, immunology, or rare diseases is especially valued.
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Rate, openings and requirements checked 2026-09-25 against micro1's own public postings.