23D AGO

Medical Writer / Clinical Document Author

micro1 / Medical Writer / Clinical Document Author

RATE

$50 - $80/HR

LOCATION

REMOTE (GLOBAL)

More micro1 jobs STEM & PhD Medical & Healthcare Writing & Creative

Apply

DESCRIPTION

Role Title: Medical Writer / Clinical Document Author 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

REQUIREMENTS

▸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.