Clinical Publications Author

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This is a fully remote position open to candidates based in United Kingdom.

Pay: $50$80/hr

Role Title: Clinical Publications Author

Role Type: Contractor

Location: Remote

We are engaging Clinical Publications Authors to participate in a customers project focused on developing advanced AI-assisted tools for medical and scientific this role youll 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.

1. Task Authoring & Review: Author and review realistic evaluation tasks based on peer-reviewed journal manuscripts scientific abstracts conference posters and presentation decks to inform AI tool development.
2. Structural & Formatting Assessment: Apply expert judgment to assess whether AI-generated draft sections align with publisher formatting standards journal guidelines and international publication ethics (such as ICMJE GPP and relevant EQUATOR Network reporting guidelines like CONSORT or STROBE).
3. Scientific Accuracy & Interpretation: Evaluate scientific accuracy in manuscripts abstracts and discussion sections distinguishing true errors in data interpretation or medical reasoning from stylistic or editorial preferences.
4. Data Verification: Trace publication claims and narratives directly to source recordssuch as Clinical Study Reports (CSRs) protocols and Tables Figures and Listings (TFLs)to verify that all statements are accurately grounded in data.
5. Structured Feedback: Provide clear and structured written rationales for each assessment enabling precise diagnosis and improvement of AI model behavior.
6. Framework Refinement: Collaborate with project leads to refine evaluation criteria and document best practices for scientific publishing workflows within AI development environments.

1. Minimum 5 years of dedicated medical/scientific publication authoring experience within a sponsor CRO MedComms agency or as an independent consultant.
2. Direct experience lead-authoring or managing peer-reviewed manuscripts published in reputable biomedical or clinical journals.
3. Strong working knowledge of publication guidelines (ICMJE GPP3/GPP2022 CONSORT) copyright compliance and journal submission workflows.
4. Demonstrated capability to interpret complex clinical data (TFLs statistical analysis plans) and translate them into clear publication-ready scientific narratives.
5. Exceptional written communication skills with a proven track record of providing actionable structured feedback on scientific draft materials.
6. Advanced degree in life sciences pharmacy or medicine (PhD PharmD MD MSc) or equivalent depth of authoring experience.
7. Therapeutic area diversity across multiple clinical phases; expertise in oncology immunology or rare diseases is especially valued.

How to apply

Apply here with your profile. We will then email you a link to complete your application on the hiring platform your application is only considered once that final step is done.