Dosing Monitor- Manhattan, NY
About The Position
IMA Clinical Research is seeking a licensed healthcare provider to serve as a Dosing Monitor for FDA-regulated clinical trials of psychedelic medications. This role involves providing direct clinical supervision and support to patients during dosing sessions as part of psychiatric investigational trials. Schedules and session lengths vary by study, with an example of a current PTSD study involving once-weekly dosing visits for 4 consecutive weeks, each session running approximately 6 hours, plus a 1-hour prep session before the first dose. Approximately 7-15 hours of study-specific training are required before each study begins. Future studies may have different visit structures, session lengths, and dosing frequencies.
Requirements
- Licensed healthcare provider
- Clinical experience providing psychotherapy outside of a research setting
- Graduate-level professional training, such as: Clinical or Counseling Psychologist (PhD/PsyD), Psychiatrist or other Physician (MD/DO), Licensed Clinical Social Worker (LCSW), Licensed Clinical Professional Counselor (LCPC), Licensed Marriage and Family Therapist (LMFT), Licensed Psychiatric Nurse Practitioner (Psychiatric NP)
Responsibilities
- Provide direct clinical supervision and support to patients during dosing sessions as part of psychiatric investigational trials with psychedelic medications.
- Conduct study-specific training.
- Adapt to varying study protocols, visit structures, session lengths, and dosing frequencies.
Benefits
- Flexibility in schedule and hours as new protocols come online.
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What This Job Offers
Job Type
Part-time
Career Level
Mid Level
Education Level
Ph.D. or professional degree
