Assistant Psychedelic Dosing Session Monitor
About The Position
Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we create an environment where meaningful work drives meaningful change. At Adams Clinical, you'll find: A culture of respect, transparency, and continuous improvement Opportunities for professional growth and learning A team dedicated to improving lives through innovation and integrity. If you're passionate about making an impact in clinical research and want to be part of a collaborative, mission-driven organization, we'd love to have you on our team. We are seeking a Part-Time 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
- At least one year of experience working for a licensed mental healthcare facility in Massachusetts, New York, Pennsylvania, or Texas
- Experience working with individuals with depression, anxiety, or other mood disorders
- Strong attention to detail for accurate observation, documentation, and reporting of dosing sessions, with strict adherence to ICH-GCP standards and protocol requirements
- 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
Nice To Haves
- Willingness to travel between regional sites is a plus, but not required (e.g., Watertown and Boston; Harlem and Bronx).
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
Job Type
Part-time
Career Level
Entry Level
Education Level
No Education Listed
