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The Senior CRA will monitor clinical trial sites for compliance, conduct site visits, train site staff, and manage relationships with stakeholders in ophthalmology.

The Senior Clinical Research Associate will manage clinical trials by conducting site visits, ensuring compliance, and contributing to study documentation.

The Clinical Research Associate will conduct site visits for clinical trials, ensuring compliance, data integrity, and safety while collaborating with site staff.

The Scientific Affairs Specialist II serves as a key liaison supporting clinical operations and client engagement, ensuring scientific rigor and alignment across global studies and laboratory services.

The Clinical Site Associate will manage site communications, support site readiness and maintain the Trial Master File, ensuring compliance and documentation accuracy.

The Scientific Affairs Specialist I supports scientific liaison activities for central laboratory services in clinical trials, ensuring scientific rigor and compliance. Responsibilities include managing test information, supporting assay selection, and collaborating with cross-functional teams.

As a Clinical Research Associate, you'll oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements, managing sites, and supporting data integrity and participant safety.

The Principal Manager, CQM leads document development and management, oversees compliance with procedures, and supports audits in clinical trials.

Oversee and manage clinical trial activities, ensuring adherence to protocols, regulatory requirements, data integrity, and participant safety. Conduct site visits, provide support, and maintain relationships with stakeholders.

Lead Clinical Research Associate will oversee and manage clinical trial sites, ensuring adherence to protocols and regulations while mentoring junior staff and ensuring data integrity.