Lexitas

The Project Specialist supports study management by facilitating site management, essential document collection, and protocol-level clinical trial documentation. They are also responsible for performing quality checks and grading ophthalmic images according to study-specific protocols.

The Director will provide strategic leadership and hands-on execution across the FDA regulatory landscape, specifically focusing on ophthalmic products. They are responsible for navigating regulatory pathways and managing interactions across CDER, CBER, and CDRH.

The Associate Director of Business Development is responsible for identifying and securing new business opportunities within the biotechnological and pharmaceutical sectors. This includes managing the sales pipeline, fostering relationships with key decision-makers, and collaborating with internal teams to formalize customer engagements.