Lead and support clinical trials as a CRA II, ensuring compliance, monitoring sites, and managing data integrity with a focus on ophthalmology studies.

This role involves site monitoring and management for clinical studies, ensuring compliance with regulations and overseeing project plans. Responsibilities include data integrity checks, training staff, managing little projects, and maintaining communication with stakeholders.

The Senior CRA 2 is responsible for site monitoring, site management, ensuring compliance with regulatory requirements, managing study activities, and leading clinical trials for the company.