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Director Psychedelic Jobs (NOW HIRING)

Collects and manages all patient data as directed * May provide expertise, training, and guidance to the community, peers, and/or students Department: School of Medicine and Public Health, Department ...

Clinical Advisor

Timonium, MD · On-site +1

$100K - $120K/yr

... therapeutics, psychedelic medicine, youth executive function, mental health parity, and other ... Reporting to the Executive Director, the Clinical Advisor will serve as the organization's senior ...

... of psychedelic-based therapies. Our people are at the heart of our progress: a diverse, highly ... The Director of Biostatistics supports the strategic design and execution of clinical trials in ...

About The Role Thesis is seeking a hands-on Supply Chain Director who can work autonomously across ... psychedelic therapy, etc.) Unlimited (yes, unlimited) Thesis nootropics A strong emphasis on ...

Supply Chain Director

New York, NY · On-site

$175K - $200K/yr

About The Role Thesis is seeking a hands-on Supply Chain Director who can work autonomously across ... psychedelic therapy, etc.) Unlimited (yes, unlimited) Thesis nootropics A strong emphasis on ...

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Director Psychedelic information

What are some common challenges faced by a Director of Psychedelic Programs when leading multidisciplinary teams?

As a Director of Psychedelic Programs, you’ll often work with diverse teams consisting of clinicians, researchers, and regulatory specialists. One common challenge is balancing the need for rigorous scientific standards with the requirements of regulatory compliance and patient safety. Additionally, fostering effective communication among professionals from different backgrounds and managing varying expectations can be demanding. Navigating the rapidly evolving legal landscape around psychedelic therapies also requires adaptability and proactive leadership to ensure ethical and compliant practices.

What does a Director of Psychedelic Programs do?

A Director of Psychedelic Programs oversees the development, management, and implementation of initiatives involving psychedelic therapies or research. This role often includes coordinating clinical trials, ensuring regulatory compliance, managing interdisciplinary teams, and guiding the overall strategy for psychedelic-assisted treatments. Directors may work in healthcare settings, research institutions, or organizations focused on mental health innovation. Their goal is to advance the safe and ethical integration of psychedelics into therapeutic or research contexts.

What are the key skills and qualifications needed to thrive as a Director of Psychedelic Programs, and why are they important?

To thrive as a Director of Psychedelic Programs, you need advanced knowledge of clinical psychology, psychiatry, or neuroscience, typically supported by a graduate degree and relevant licensure. Familiarity with clinical research protocols, regulatory compliance, and electronic data management systems is crucial. Exceptional leadership, ethical judgment, and strong communication skills help foster collaboration among multidisciplinary teams and stakeholders. These skills ensure safe, effective program delivery, uphold ethical standards, and support successful clinical outcomes in this emerging field.
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Infographic showing various Director Psychedelic job openings in the United States as of June 2026, with employment types broken down into 70% Full Time, 20% Part Time, and 10% Contract. Highlights an 90% In-person, and 10% Remote job distribution.

Licensed Therapist & Psychedelic Session Monitor

The Remedy Mental Health

Golden Valley, MN

Full-time

Medical, Dental, Vision, Life, Retirement

Posted yesterday


Job description

Mental health challenges can make simple things feel hard, and hard things feel impossible. At The Remedy Mental Health, we recognize the profound impact compassionate care can have and we meet our patients wherever they are on their journey. With locations across the Twin Cities, Western Wisconsin, and South Dakota our mission is to make exceptional mental health care accessible to all.

We are at the forefront of a new era in mental health treatment. In addition to delivering evidence-based outpatient therapy, our clinicians participate in pioneering psychedelic-assisted therapy clinical trials placing The Remedy among a select group of clinical sites shaping the future of psychiatric medicine.

This is not a traditional therapy position. You will carry a meaningful outpatient caseload and serve as a certified Psychedelic Session Monitor within FDA-regulated Phase II and Phase III investigational drug trials and be among the first clinicians in the country to combine conventional psychotherapy with emerging psychedelic-assisted interventions.

  • Dual clinical identity: licensed outpatient therapist and credentialed clinical trial monitor.
  • Hands-on experience with investigational psychedelic compounds under FDA and GCP oversight.
  • Professional development including trauma-informed care and psychedelic therapy certification support.
  • Collaborative interdisciplinary team with weekly case consultation and direct principal investigator access.
  • Hybrid schedule: in-person dosing sessions balanced with in-person and telehealth for standard outpatient care.

The Licensed Therapist & Clinical Trial Specialist carries an active outpatient caseload while serving as a trained monitor within The Remedy's psychedelic-assisted therapy research program. The clinical trial component requires the therapist to provide direct participant supervision during investigational substance administrations, maintain detailed source documentation, and deliver preparatory and integration psychotherapy as defined by each study protocol.

Outpatient Clinical Practice

  • Conduct diagnostic assessments and formulate individualized, evidence-based treatment plans.
  • Provide individual psychotherapy in person and via telehealth, adjusting approaches to meet each client's evolving needs.
  • Maintain timely, accurate clinical records and progress notes within the EHR system
  • Participate in weekly interdisciplinary team meetings and contribute to a collaborative clinical culture.
  • Utilize creative, client-centered interventions to support goal attainment and sustainable recovery.

Psychedelic Clinical Trial Duties

  • Serve as a Psychedelic Session Monitor within FDA-regulated Phase II and Phase III investigational drug trials, working as part of a two-person supervision team.
  • Maintain a safe, supportive physical and emotional environment for participants throughout extended dosing sessions (8+ hours).
  • Execute therapeutic and supportive frameworks with fidelity to ensure data consistency across the trial.
  • Conduct structured preparation sessions prior to dosing days to build participant rapport and informed expectations.
  • Facilitate post-experience integration sessions to support participants in processing their observations.
  • Complete detailed clinical observations and source documentation in compliance with GCP guidelines and Human Subject Protection regulations.
  • Maintain all required DEA registrations and state-specific certifications for controlled substance handling in a research context.

Required Qualifications

  • Master's degree or higher in a behavioral science or related field from an accredited institution.
  • Independently licensed or licensure-eligible as 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.

What We Offer

  • Medical, dental, and vision insurance.
  • Health Savings Account (HSA).
  • 401(k) with employer match.
  • Life insurance and AD&D coverage.
  • Short-term disability insurance.