Sr. Associate, Clinical Data Management & Operations

About the role

The Sr. Associate, Clinical Data Management & Operations supports Alcon’s Research & Development team by providing scientific, operational, and analytical assistance for clinical research activities in ophthalmology and vision science.

Key responsibilities

• Process, review, and organize clinical data and records to ensure accuracy and timely availability.
• Assist in oversight and reporting of clinical studies, including protocol, statistical analysis plan, and study report reviews.
• Develop case report form (CRF) templates and study‑specific data capture tools.
• Perform data entry, source‑to‑CRF verification, and routine/ad‑hoc data quality checks.
• Analyze scientific data from studies and literature; contribute to publications, abstracts, posters, and presentations.
• Compile competitive intelligence from conferences, journals, and internal sources.
• Prepare narrative summaries, literature reviews, and scientific slide decks.
• Coordinate study agreements, CTRI registrations, IRB submissions, and equipment training with investigators.
• Monitor study progress, compliance, and manage payment milestones.
• Lead ancillary supplies logistics, including import, transportation, and storage.
• Follow GxP requirements, SOPs, and maintain complete documentation.

Required profile

• Bachelor’s degree with relevant experience or a Master’s/PhD in Vision Science or related field.
• Fluent English communication skills.
• Master’s degree in Optometry, Ophthalmology, or Vision Science.
• Minimum 2 years experience in clinical study documentation and operational support.
• Minimum 2 years experience planning, conducting, and reporting clinical research in optometry, ophthalmology, or vision science.
• Background in intraocular lenses, physiological optics, or related areas.

Required skills