Assistant Psychedelic Dosing Session Monitor
About The Position
Adams Clinical is seeking a per diem Assistant Psychedelic Dosing Monitor 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. In this role, you will support dosing sessions under the supervision of the Lead Dosing Session Monitor, ensuring participant safety and protocol adherence throughout the trial. You'll collaborate with a multidisciplinary clinical team, complete study-specific training, and uphold rigorous ICH-GCP standards to support data integrity and participant wellbeing. Willingness to travel between regional sites is a plus, but not required (e.g., Watertown and Boston; Harlem and Bronx).
Requirements
- Minimum of 1 year of experience in a mental healthcare setting including clinical research experience as a Clinical Research Coordinator or in a comparable role supporting psychiatric research studies
- Bachelors degree from accredited institution; Clinical sciences, Psychology or Nursing focus is a plus
- 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
Nice To Haves
- Prior experience with industry-sponsored psychedelic clinical trials (e.g., Compass, Cybin, MindMed, Atai)
Responsibilities
- Serve as Assistant Dosing Session Monitor in onsite psychedelic clinical trials for depression, anxiety, and other mood disorders.
- Complete study-sponsored 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.
- Fulfill additional responsibilities including administrative tasks, onboarding, and study-related training as assigned.
Benefits
- 401(k) matching
- Employee assistance program
- Paid time off
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What This Job Offers
Career Level
Entry Level
