YO HR Consultancy

Role Title: Medical Writer / Clinical Document Author
Role Type: Contractor
Location: Remote
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
<ul>
<li>Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.</li>
<li>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.</li>
<li>Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.</li>
<li>Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.</li>
<li>Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.</li>
<li>Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.</li>
</ul>
Preferred Qualifications
<ul>
<li>Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.</li>
<li>Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.</li>
<li>Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.</li>
<li>Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.</li>
<li>Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.</li>
<li>Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.</li>
<li>Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.</li>
</ul>
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.