An opportunity is available for a Medical Writer (Pharmaceutical) to support AI development and evaluation projects. There are currently 30 openings available.
Job Responsibilities
- 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.
Compensation: $30 - $60/hr.
Location / Region: Remote.
Relevant skills include:
- 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
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