Adams Clinical Benefits Overview

Conduct pharmaceutical-sponsored clinical trials under physician and nursing supervision. Responsibilities include IV placement and infusions, injections, phlebotomy, medical record and laboratory review, adverse-event reporting, medication reconciliation, emergency support, informed consent, screening, data entry, regulatory binder maintenance, and mentoring clinical research coordinators. The role requires compliance with FDA regulations and GCP guidelines and regular work across two New York City-area locations.

The Lead Dosing Session Monitor will act as the primary therapist during psychedelic clinical trials, providing support to participants and collaborating with clinicians.

The Assistant Psychedelic Dosing Session Monitor supports psychedelic clinical trials, ensuring participant safety and protocol adherence while collaborating with clinicians and site staff.