Sr. Associate, Clinical Research (Non-MD)

Key Responsibilities: 1. Author, co-author, and support updates to CEPs, CERs, PMCF Plans and Reports, SLR protocols/reports, and related clinical evaluation documentation for assigned medical device products. 2. Apply clinical evaluation requirements, internal procedures, templates, and evidence appraisal expectations to produce clear, traceable, scientifically sound, and audit-ready deliverables. 3. Ensure clinical evaluation deliverables are developed in alignment with EU MDR 2017/745 , appl…