Licensed Therapist & Lead Psychedelic Session Monitor

The Remedy • Golden Valley, MN

2d • $18,000 - $94,000 • Hybrid

About The Position

The Licensed Therapist & Clinical Trial Specialist maintains an outpatient caseload while serving as a trained monitor in The Remedy Mental Health’s psychedelic-assisted therapy research program. The position combines conventional outpatient psychotherapy with participation in FDA-regulated Phase II and Phase III investigational drug trials. The therapist provides direct participant supervision during investigational substance administrations, keeps detailed source documentation, and delivers preparation and integration psychotherapy as specified by each study protocol.

The outpatient role includes diagnostic assessment, individualized treatment planning, psychotherapy delivered in person and through telehealth, timely EHR documentation, and participation in interdisciplinary team meetings. In clinical trials, the therapist works as part of a two-person supervision team, supports participants throughout extended dosing sessions of eight or more hours, follows study frameworks, conducts preparation and integration sessions, and documents observations in accordance with GCP and Human Subject Protection requirements. The role also requires applicable DEA registrations and state-specific certifications for controlled-substance handling in research.

Requirements

• Master’s degree or higher in behavioral science or a related field from an accredited institution.
• Independently licensed or licensure-eligible as an LPCC, LMFT, LICSW, or LP in Minnesota.
• 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 during extended dosing sessions of eight or more hours.
• Follow therapeutic and supportive frameworks with fidelity to support data consistency across the trial.
• Conduct structured preparation sessions before dosing days to build participant rapport and establish 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 access to the principal investigator.
• Hybrid schedule balancing in-person dosing sessions with in-person and telehealth outpatient care.

What This Job Offers

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