Per Diem Lead Dosing Session Monitor

Adams Clinical•Philadelphia, PA

9d•Hybrid

About The Position

Adams Clinical is a rapidly growing research site network specializing in late-phase industry-sponsored trials of novel treatments for a variety of psychiatric and neurological conditions. We are seeking a Per Diem Lead Dosing Monitor/Therapist for exciting clinical trials focused on psychedelic research for individuals with depression, anxiety, and other mood disorders at one or more of our research site locations. Willingness to travel between regional sites is a plus but not required.

Requirements

Licensed mental health professional in Massachusetts, New York, Pennsylvania, or Texas (e.g., PsyD, PhD, LCSW, LMSW, LMHC, LMFT), with the ability to provide psychotherapy in compliance with state regulations
Attention to detail is critical for this role to ensure accurate observation, documentation, and reporting of dosing sessions, with strict adherence to ICH-GCP standards and protocol requirements.
Experience working with individuals with depression, anxiety, or other mood disorders
Strong interpersonal and communication skills, with an interest in advancing mental health care in a clinical research setting.
Ability to meet fixed scheduling expectations, including consistent on-site availability.
Final candidate must be approved by both Adams Clinical and the study sponsor.
Willingness to learn and adhere to ICH-GCP standards.
Provide documentation verifying identity and authorization to work in the United States and complete Form I-9 within the required timeframe.

Nice To Haves

Willingness to travel between regional sites is a plus but not required.

Responsibilities

Serve as Lead Study Therapist in psychedelic clinical trials for depression, anxiety, and other mood disorders.
Complete study-sponsored therapist training, and Adams Clinical site-specific training requirements.
Provide support to participants throughout the clinical trial in alignment with the study protocol and training guidelines.
Collaborate with clinicians and site staff managing participant participation in the study.
Administrative tasks, onboard, and study-related training, as well as other tasks assigned.