- Esperienza
- Qualsiasi
- Stipendio
- 50 USD – 50 USD / ora
- Aperture
- 1
- Pubblicato
- 1 settimana fa
- Modalità di lavoro
- Lavoro da casa
- Requisiti di ammissibilità
- Professionals with expertise in pharmaceuticals, drug development, clinical research, or clinical trials are encouraged to apply.
- Riprendere
- È necessario candidarsi
Descrizione del lavoro
Role Overview
Bring your pharmaceutical and clinical trial knowledge to a specialized visual-document review initiative. The work centers on building strong assessment tasks and benchmark materials that are accurate, objective, and useful for evaluation.
What You Will Be Doing
- Create advanced, domain-specific tasks from pharmaceutical and clinical trial documents.
- Examine visual documents and define expected outputs that are clear and evidence-based.
- Build objective grading rubrics with measurable criteria for success.
- Check task quality to keep outputs accurate, consistent, and relevant to the domain.
- Contribute to the creation of structured benchmarks for document understanding and instruction-following evaluation.
Who We Are Looking For
- Experienced professionals with strong exposure to pharmaceuticals, drug development, clinical research, or clinical trials.
- Solid knowledge of clinical trial records, regulatory documents, and research processes.
- Ability to design precise, evidence-backed tasks with unambiguous expected results.
- Strong analytical ability and a sharp eye for detail.
- Excellent written communication skills and the capacity to work in a structured evaluation format.
Role Details
This is a remote, part-time contract engagement. The work is project-based and ongoing.
Compensation is $50 per hour.
Application Process
- Use the Easy Apply option to submit your application.
- Only shortlisted candidates will be contacted with the next steps.