Jamie Thompson

I’m a Clinical Trial Director with over 8 years of hands-on experience in clinical trial coordination, regulatory compliance, and site management. I help teams maintain inspection-ready studies while building strong quality processes that protect patients and support successful recruitment.

Since June 2020, I’ve provided clinical research expertise in the design and implementation of multiple multi-site trials, including research infrastructure development like the creation and maintenance of an eRegulatory binder and quality control processes. I coordinate across multiple sites, communicating status, risks, and improvement areas to leadership, and I develop and review core study documents such as informed consents, case report forms, and protocol-specific tools.

I’m known for applying Good Clinical Practice (GCP) guidelines in daily operations—maintaining current GCP certification—and ensuring compliance with FDA, IRB, and HIPAA regulations. I also train staff on research policies, procedures, and regulatory requirements, and I collaborate with CRCs and site management to support recruitment efforts.