-Responsible for management of all site-specific study operations, taking full responsibility for participant care, longitudinal follow-ups, scheduling, and regulatory documentation.

-Provides clinical research leadership, operational oversight, and serves as a subject matter resource for staff regarding regulatory compliance, GCP, SOPs, protocol adherence, and quality expectations to ensure studies are conducted efficiently.

-Requires the ability to balance a primary focus on clinical research with direct patient care, rapidly shifting priorities to meet workflow demands in a fast-paced setting.

-Willingness to obtain required Protecting Human Subjects training and Good Clinical Practice certifications within the first month of employment.

**PURPOSE AND SCOPE:**

Supports the Organization mission, vision, core values and customer service philosophy. Adheres to the Organization Compliance Program, including following all regulatory and Organ...