Clinical Research Psychedelic Therapist/Psychometric Rater
Tekton Research · tektonresearch.com
St. LouisContract
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The job in short
Psychedelic therapy psychometric rater for clinical research.
Clinical
Details
- Found
- 10 d ago · posted 2026-10-20
- Location as listed
- St. Louis, MO, US
- Role
- Behavioral Health / Therapist
- Source
- The company’s own careers site
Full description
Tekton Research is looking for an experienced clinical research Clinical Research Psychedelic Therapist and/or Psychometric Rater in St. Louis, Missouri to join our team!
St. Louis, Missouri | Full-Time or Contract | On-Site
Position: We are seeking an independently licensed social worker or mental health professional for a contract or full-time role. The selected candidate will receive research training and learn to serve as a psychedelic therapist and psychometric rater.
The professional will complete approximately 40 hours of training and earn certification for work in psychedelic research. The role also offers an opportunity to become a Psychometric Rater, responsible for interviewing research participants and their informants or caregivers as part of eligibility evaluations for studies involving various health conditions. Candidates must be professional, respectful, self-motivated, dependable, and committed to a strong work ethic and high integrity.
Job Description:
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Review participants’ medical histories, meet with prospective participants, gather information, and conduct assessments before and after psychedelic dosing days.
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Full-time employees may also be trained to administer a variety of psychometric rating scales in clinical trials involving conditions such as ADHD, Alzheimer’s disease, bipolar disorder, generalized anxiety disorder, major depressive disorder, post-traumatic stress disorder, substance use disorders, epilepsy, anxiety disorders, and schizophrenia or schizoaffective disorder.
Required Skills/Abilities:
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Proficiency with Microsoft applications, email, electronic health records, and web-based tools, along with a typing speed of at least 40 words per minute.
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Strong organizational skills, attention to detail, and written, verbal, interpersonal, and listening abilities.
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Ability to work effectively both independently and collaboratively with coworkers, participants, managers, and external customers.
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Capacity to manage multiple tasks, adapt to changing workloads and priorities, solve problems with minimal supervision, and protect highly sensitive information.
Education and Experience:
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A relevant master’s degree and independent professional license are required.
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A relevant PhD degree strongly preferred
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1+ years' experience performing psychometric rating scales in a clinical setting or for clinical trials, or an equivalent combination of education and experience is required.
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Current or previous certifications to rate the following scales is highly preferred: SCID-5-CT, MINI, LSAS, HAM-A/D, C-SSRS, MADRS, MGH-ATRQ, ISI, NPI, CGI, HDRS-17, PANSS, YMRS, MMSE, ADAS-COG, CDR, RBANS, and MOCA.
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Bi-lingual (English / Spanish) proficiency is a plus.
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Experience as a Clinical Research Coordinator at a research site is a plus.
Physical Requirements:
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Prolonged periods of sitting at a desk and working on a computer
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Must be able to lift up to 15 pounds at times
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