We are sharing a specialised part-time consulting opportunity for professionals experienced in pharmaceutical documentation, clinical trial materials, study protocol review, regulatory-style records, clinical research workflows, instruction-based task design, and structured evaluation.
This role supports current and upcoming remote consulting opportunities focused on AI-assisted review of pharmaceutical and clinical research documents, forms, tables, study materials, and related visual content. Selected professionals will create complex evaluation tasks using clinical trial and pharma-related materials, define clear expected answers, and develop objective rubrics for assessing response accuracy, instruction alignment, and domain understanding.
Key Responsibilities
Professionals in this role may contribute to:
Clinical Research Task Development