Licensed Therapist & Lead Psychedelic Session Monitor

The Remedy • Golden Valley, MN

20h • Hybrid

About The Position

The Licensed Therapist & Lead Psychedelic Session Monitor carries an active outpatient caseload while serving as a trained monitor in The Remedy Mental Health’s psychedelic-assisted therapy research program. The role combines evidence-based outpatient psychotherapy with direct participant supervision during investigational substance administrations in FDA-regulated Phase II and Phase III clinical trials. Trial responsibilities include preparation and integration psychotherapy, detailed source documentation, and adherence to study protocols and applicable research regulations. The position involves in-person dosing sessions and a mix of in-person and telehealth outpatient care. The schedule is Monday through Friday, 8:00 a.m. to 5:00 p.m.

Requirements

• Master’s degree or higher in a behavioral science or related field from an accredited institution.
• Independently licensed or licensure-eligible in Minnesota as an LPCC, LMFT, LICSW, or LP.
• Experience completing diagnostic assessments, treatment plans, and clinical progress notes.
• Ability to remain present and attentive during extended monitoring sessions.

Responsibilities

• Conduct diagnostic assessments and formulate individualized, evidence-based treatment plans.
• Provide individual psychotherapy in person and via telehealth, adapting approaches to clients’ evolving needs.
• Maintain timely and accurate clinical records and progress notes in the EHR system.
• Participate in weekly interdisciplinary team meetings and contribute to a collaborative clinical culture.
• Use creative, client-centered interventions to support goal attainment and sustainable recovery.
• Serve as a Psychedelic Session Monitor in FDA-regulated Phase II and Phase III investigational drug trials as part of a two-person supervision team.
• Maintain a safe, supportive physical and emotional environment for participants throughout extended dosing sessions of 8+ hours.
• Follow therapeutic and supportive frameworks with fidelity to ensure consistency across the trial.
• Conduct structured preparation sessions before dosing days to build rapport and set informed expectations.
• Facilitate post-experience integration sessions to help participants process their observations.
• Complete detailed clinical observations and source documentation in compliance with GCP guidelines and Human Subject Protection regulations.
• Maintain required DEA registrations and state-specific certifications for controlled substance handling in a research context.

Benefits

• Medical, dental, and vision insurance.
• Health Savings Account (HSA).
• 401(k) with employer match.
• Life insurance and AD&D coverage.
• Short-term disability insurance.
• Professional development, including trauma-informed care and psychedelic therapy certification support.
• Weekly case consultation and direct principal investigator access.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level