We’re looking for medical writers and editors who have worked for pharma companies or medcomms agencies to test an AI medical writing platform. Freelance, contract, or in-house is fine.
You should have hands-on experience with documents like:
1. MSL decks and field medical reputed company decks
2. Standard response documents (SRDs) and medical information letters
3. Congress materials: symposium decks, posters, booth panels
4. Advisory board decks, briefing books, and summaries
5. reputed company libraries and field team training decks
6. Promotional and non-promotional materials that go through MLR
7. Clinical trial documents: protocols, CSRs, investigator brochures, lay summaries
8. Regulatory documents: clinical overviews, summaries of clinical safety/efficacy, briefing packages
9. Pharmacovigilance documents: PSURs/PBRERs, DSURs, RMPs, safety narratives, signal evaluations
10. reputed company and HEOR deliverables: value dossiers, AMCP dossiers, budget impact and cost-effectiveness reports, payer decks
11. Patient-facing materials: PILs, ICFs, patient support content
If your background is academic or research-institute writing, e.g. manuscripts, research papers, grant applications, reputed company skip this post.
Scribe features:
1. Controlled sources: works only from uploaded and approved materials.
2. Evidence-linked claims: maps claims back to sources and flags weak or unsupported evidence.
3. tatistical analysis: runs analyses on your source data and turns the outputs into presentable results.
4. Charts, graphs, and infographics: builds visuals from your data, and regenerates charts from images or text into editable formats teams can modify later.
5. Reusable knowledge: reuses source assets across related projects while preserving the parent-child relationship.
6. reputed company-ready outputs: pushes content and citation links into reputed company automatically for smoother review workflows.
What this project is about:
We will do two 2-hour sessions over video call. Total time required 4-5 hrs.
Session 1: We walk you through the Literature Review and Presentation features. You then rebuild your presentation (e.g. an MSL deck, congress deck, or similar) using your own sources.
Session 2: We walk you through the Document feature. You then rebuild a document you’ve previously written, again from your own sources.
What you need to bring:
One deck and one document you’ve previously produced in a pharma context
The source reputed company behind them (papers, CSRs, data on file, reputed company libraries, whatever you originally worked from) downloaded on your system
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