Part Time Dosing Session Monitor

Adams Clinical is a leading clinical trial site network committed to accelerating the development of life‑changing medicines. Our mission is to deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. We foster a culture of respect, transparency, and continuous improvement, offering opportunities for professional growth and a team dedicated to improving lives through innovation and integrity.

About the role

We are seeking a Part‑Time Psychedelic Dosing Monitor / Therapist to support 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.

Responsibilities

• Serve as Lead Study Therapist in 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.
• Maintain accurate observation, documentation, and reporting of dosing sessions, adhering to ICH‑GCP standards and protocol requirements.
• Perform administrative tasks, onboarding, study‑related training, and other assigned duties.

Qualifications

• Licensed mental health professional in New York (e.g., PsyD, PhD, LCSW, LMSW, LMHC, LMFT) authorized to provide psychotherapy in compliance with state regulations.
• Attention to detail for accurate observation, documentation, and reporting.
• Experience working with individuals with depression, anxiety, or other mood disorders.
• Strong interpersonal and communication skills with 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.
• Preferred: Prior experience with industry‑sponsored psychedelic clinical trials.

Commitments

• Part‑time role with 24 guaranteed hours per week.
• Therapists must maintain consistent availability three days per week for participant‑facing responsibilities (pre‑dose preparations, monitoring during dosing sessions, post‑dose follow‑ups). Availability must be either Monday‑Wednesday or Tuesday‑Thursday.
• Scheduling based on study volume, participant availability, and internal priorities; dependable adherence to assigned days required.
• Majority of participant visits conducted on‑site, with some remote visits.
• Therapists must be willing to learn and adhere to ICH‑GCP standards.

Pay

$60.00 – $76.00 per hour

Benefits

• 401(k) matching
• Professional development assistance