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The Senior Clinical Research Associate will monitor clinical studies, ensuring compliance with protocols, regulations, and procedures, while also overseeing remote and on-site clinical trial progress.

As a Senior Clinical Research Associate, you will monitor clinical studies, ensuring compliance with protocols and regulatory requirements. You will work both on-site at investigative sites and remotely, focusing on data integrity and patient safety.

The Senior Clinical Research Associate will manage clinical trials, ensuring compliance, data integrity, and patient safety while collaborating with investigators and site staff.

As a Study Start Up Specialist, you will conduct feasibility assessments, site identification and negotiations, ensuring compliance with regulations while driving study initiation success.