Sr.Associate-ClinicalProjectsCoordinator

**Summary of Position:** This role is part of Alcon’s Research & Development organization - a team that innovates boldly to deliver products and services that revolutionize eye care, advance patient outcomes, and help people see brilliantly. The Sr. Associate, Clinical Data Management & Operations provides scientific, operational, and analytical support for clinical research activities. The role is responsible for supporting the planning, conduct and analysis of research agreements, clinical studies for new product development and/or post market studies. This position partners closely with internally with cross‑functional stakeholders and externally with sites to ensure compliant, high‑quality, and on‑time delivery of medical evidence generation. **Key Responsibilities:** * Support in processing, review, and organization of clinical data and records, ensuring accuracy, consistency, and timely availability for analysis and reporting. * Assist in oversight and reporting of clinical studies including review of clinical research protocols, statistical analysis plans, and study reports to ensure data integrity, scientific rigor, and regulatory compliance. * Assist in developing case report form (CRF) templates and study-specific data capture tools. * Perform data entry and source‑to‑CRF verification; execute routine and ad‑hoc data quality checks. * Review and critically analyze scientific data from clinical studies as well as from published literature. * Support/contribute to impactful peer‑reviewed publications, abstracts, posters, and presentations. * Compile competitive intelligence (CI) from optometry, ophthalmology and vision science conferences, scientific literature, ophthalmology journals, and internal CI sources. * Prepare narrative summaries, literature reviews, and scientific slide decks on topics of interest. * Coordinate with investigators on study agreement preparation, CTRI registrations, IRB submissions, clinical study equipment training. * Monitor study