Medical Writer (Pharmaceutical)
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.
- Pay
- Firm hourly pay: $30 - $60/hour
- Location
- Remote
- Eligibility
- Remote, applicant location not specified
- Qualification difficulty
- Highly selective
How current is this information?
The public role and application path were checked. Details can still change; this is not an endorsement or guarantee.
- Platform
- Micro1
- Fit category
- General professional
- Listing/source checked
- Sep 21, 2026
- Apply link checked
- Sep 21, 2026
Application
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What this role involves
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.
What you’d do
- 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.
What they’re looking for
Before you apply
Review the main fit signals and unresolved details before opening the platform.
Why it may fit
- Applicants whose experience directly matches the current Medical Writer (Pharmaceutical) qualifications.
- Professionals eligible for the stated Micro1 location and remote-work conditions: Remote.
Check before applying
Reasons to pause
- You cannot meet the public role's stated location or eligibility requirements.
- You need guaranteed acceptance, hours, pay, or project duration.
Still to verify
- Review the current Micro1 job post before applying. Role type, contractor status, location, screening steps, pay text, hours, and availability can change.
- Applicant eligibility still needs checking: Remote, applicant location not specified.
What to prepare
- 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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