Catalogue update: this role is no longer listed in the current micro1 catalogue. Browse current AI Training opportunities.
About the role
Contribute specialist knowledge to an AI project focused on Medical Writer / Clinical Document Author. The client uses professional input to assess and improve the quality of model performance.
Skills and focus areas
regulatory medical writing · clinical study report authoring · ich e3 guidelines · scientific accuracy assessment · source data verification · clinical protocol interpretation · tfl (tables, figures, listings) analysis · written communication · structured feedback provision · collaborative problem-solving · ai-assisted documentation evaluation · periodic safety documentation (ich e2f, ich e2c) · ectd (electronic common technical document) knowledge · oncology and haematology domain expertise
What you will do
- Construct realistic assessment problems grounded in professional practice.
- Build or assess financial analyses, checking assumptions and the business implications.
- Apply clinical judgment to cases, documentation or model responses and explain the evidence.
- Produce clear professional documentation that makes reasoning and decisions understandable.
Experience and requirements
- Relevant areas of expertise: regulatory medical writing, clinical study report authoring, ich e3 guidelines, scientific accuracy assessment.
- The client specifies: “Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.”
Working arrangements
- The engagement is offered on a contractor basis.
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