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Clinical Research Psychedelic Therapist/Psychometric Rater

Tekton Research · tektonresearch.com
St. LouisContract
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Psychedelic therapy psychometric rater for clinical research.

Clinical

Details

Found
15 d ago · posted 2026-10-20
Location
St. Louis, MO, US

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: • Review participants’ medical histories, meet with prospective participants, gather information, and conduct assessments before and after psychedelic dosing days. • 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: • Proficiency with Microsoft applications, email, electronic health records, and web-based tools, along with a typing speed of at least 40 words per minute. • Strong organizational skills, attention to detail, and written, verbal, interpersonal, and listening abilities. • Ability to work effectively both independently and collaboratively with coworkers, participants, managers, and external customers. • Capacity to manage multiple tasks, adapt to changing workloads and priorities, solve problems with minimal supervision, and protect highly sensitive information. Education and Experience: • A relevant master’s degree and independent professional license are required. • A relevant PhD degree strongly preferred • 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. • 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. • Bi-lingual (English / Spanish) proficiency is a plus. • Experience as a Clinical Research Coordinator at a research site is a plus. Physical Requirements: • Prolonged periods of sitting at a desk and working on a computer • Must be able to lift up to 15 pounds at times

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