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The HEOR Scientist develops strategies for health outcomes research, drives study execution, influences project management, and disseminates findings to enhance patient outcomes across life cycles.

As a Clinical Research Associate II, you will conduct and monitor clinical trials, ensuring compliance, data integrity, and patient safety. You'll collaborate with site staff, perform data reviews, and prepare study documents.

The Supplier Performance Manager will manage supplier-specific objectives, coordinate projects, foster relationships, and oversee vendor activities in clinical research.

As a Senior Clinical Research Associate, you will oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements while managing site performance and collaborating with cross-functional teams.

As a Clinical Research Associate, you will conduct various trial visits, ensure protocol compliance, and collaborate with investigators to maintain data integrity and patient safety.

Monitor clinical trial sites for compliance, conduct site visits, manage multiple projects, train site staff, and ensure data integrity in ophthalmology studies.

The Senior Clinical Research Associate will oversee clinical trials, ensuring compliance, maintaining data integrity, and preparing study documentation while collaborating with investigators and site staff.

As a Clinical Research Associate, you will conduct clinical trial monitoring, ensure protocol compliance, analyze data, and collaborate with site staff.

The Clinical Research Associate will conduct monitoring visits for clinical trials, ensuring compliance and data integrity, and preparing study documentation.

The Clinical Research Associate will conduct site visits, ensure compliance and patient safety, and review clinical data with a focus on trial operations.