Principal, Clinical Research (Clinical Project Lead – PMCF and Lifecycle Management, Instrumentation)
Alcon · Posted Nov 5, 2026
- Bangalore, India
- Senior
- 5+ years
Lead post‑market clinical follow‑up and lifecycle management for ophthalmic instrumentation, ensuring compliance with EU MDR and related regulations.
Responsibilities
- Plan and execute PMCF activities including registries, surveys, retrospective analyses and real‑world evidence initiatives
- Develop protocols and reports aligned with EU MDR, MDCG guidance and internal procedures
- Interpret PMCF findings against device performance, safety trends and benefit‑risk conclusions
- Conduct clinical review of evaluation documentation, including reports, assessments and evidence gap analyses
- Assess clinical impact of product changes and safety signals
Requirements
- Bachelor’s degree in a scientific, clinical, engineering, or related field
- Advanced degree in vision science, ophthalmology, optometry, clinical research or related discipline
- Nice to have: Advanced degree in vision science or related field
- Nice to have: Experience supporting EU MDR clinical documentation or regulatory reviews
- Nice to have: Ophthalmic clinical practice experience