Dosing Monitor- Manhattan, NY

Dosing Monitor (DM) Clinical Research

IMA Clinical Research is seeking a licensed healthcare provider to serve as a Dosing Monitor for FDA-regulated clinical trials of psychedelic medications, including an active PTSD study, with an upcoming second PTSD study and two MDD studies also requiring DM coverage.

As a Dosing Monitor, you'll provide direct clinical supervision and support to patients during dosing sessions as part of psychiatric investigational trials with psychedelic medications. Schedules vary by study for example, our current PTSD study involves once-weekly dosing visits for 4 consecutive weeks, with each dosing session running approximately 6 hours, and a 1-hour prep session before the first dose. There is also ~7-15 hours of study-specific training before each study begins. Future studies may involve different visit structures, session lengths, and dosing frequencies depending on the sponsor and protocol.

Compensation: $200 - $250 an hour depending on experience and licensure

Must-Have Qualifications:

• Licensed healthcare provider with clinical experience providing psychotherapy outside of a research setting, and 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)

This is an opportunity to be at the forefront of psychedelic research, working across multiple sponsor studies in a variety of psychiatric indications as our program grows. Schedule and hours are study-dependent, offering flexibility as new protocols come online.

Interested candidates should apply to be considered as we build our roster of qualified Dosing Monitors for current and upcoming studies.