Teams at Adams Clinical

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.

Provides entry-level support for clinical trial operations under supervision. Responsibilities include participant scheduling and liaison activities, visit preparation, vital signs, ECGs, specimen collection, source documentation, EDC data entry, query resolution, study binder maintenance, medical records management, investigational product accountability, and monitoring visit support. Ensures compliance with protocols, ICH-GCP, site SOPs, regulatory requirements, and audit-readiness standards.

Support onsite psychedelic dosing sessions under a Lead Monitor’s supervision, ensuring participant safety and protocol adherence. Complete study and site training, collaborate with clinical staff, observe and document dosing sessions per ICH-GCP, perform administrative onboarding tasks, and maintain consistent on-site availability (three days/week). May travel between regional sites as needed.