Regulatory Coordinator

Advarra has been at the forefront of clinical research for over 35 years, providing essential services that enhance the effectiveness and efficiency of clinical trials. Established in 1983, the company has evolved from its roots in ethical review to become a premier provider of a broad range of services including Institutional Review Board (IRB) reviews, consulting services, data monitoring, and research compliance. Today, Advarra plays a critical role in advancing human health by facilitating the safe and ethical development of new therapies.

Headquartered in Columbia, Maryland, Advarra operates within a deeply connected ecosystem that brings together patients, clinical researchers, sponsors, and CROs. This connected approach allows the company to accelerate clinical research processes, ensuring rapid and reliable results while maintaining a strong commitment to patient safety and ethical integrity. Advarra's advanced technology solutions empower investigators and sponsors by simplifying data management, optimizing patient engagement, and enhancing the visibility of trial metrics. By consistently prioritizing innovation, Advarra not only addresses the challenges of today’s clinical research landscape but also anticipates the needs of tomorrow, making it a trusted partner for clinical research advancements across the globe.