Jobs at Meril

Develops and writes clinical evaluation reports for pre- and post-market medical devices. The role involves evaluating clinical, scientific, and medical data; interpreting regulations and standards; drawing evidence-based conclusions; ensuring compliance with SOPs and quality requirements; and supporting clinical, regulatory, quality, and engineering projects. The position also requires project management, clear scientific communication, independent work, and collaboration with executives, research sites, and research subjects.

Develops and writes clinical evaluation reports for pre- and post-market medical devices. Reviews and analyzes clinical trial, literature, and real-world data; interprets regulations and standards; draws evidence-based conclusions; and ensures document quality and compliance with SOPs. The role also supports clinical, regulatory, quality, and engineering projects while communicating scientific content clearly and managing deliverables on time and within budget.