Adams Clinical Benefits Overview

Provide administrative and regulatory support for clinical trials: prepare and maintain study documents and regulatory files, assist with IRB submissions and renewals, track staff training/certifications, and help ensure records are audit-ready and compliant with applicable regulations.

Support participant evaluation, triage, and enrollment for clinical trials. Prepare study materials, assist prescreening and informed consent, collect demographics and basic clinical data, perform vitals and lab collections (training provided), maintain source documentation, and enter data into EDC systems to ensure compliant, efficient study operations.

The Psychedelic Dosing Monitor facilitates on-site and remote support for participants in psychedelic clinical trials, ensuring safety and protocol adherence while providing therapy for mood disorders.