Responsibilities

The Clinical Research Associate will conduct and coordinate various aspects of clinical monitoring and site management, including performing remote or on-site visits to assess protocol and regulatory compliance, managing required documentation, and ensuring data accuracy through review of source documents. They will also assess investigational products, document observations in reports, escalate deficiencies to clinical management, and maintain regular contact with investigative sites to ensure protocol adherence and issue resolution, while actively contributing to audit readiness and developing collaborative relationships with investigational sites.