Longmont, Colorado, United States · On-site
Position: Psychometric Rater (Full-Time/Exempt) The Psychometric Rater will be responsible for interviewing research participants and their informants/caregivers, who are being evaluated to participate in a research stud…
Skills: Psychometric Rating, Clinical Trial Protocol, Patient Interviewing, Medical History Review, GCP Compliance
Edmond, Oklahoma, United States · On-site
Position Summary The Clinical Research Coordinator (CRC) is responsible for coordinating and managing clinical research studies while ensuring compliance with study protocols, Good Clinical Practice (GCP), FDA regulation…
Skills: Clinical Trial Management, Regulatory Compliance, Protocol Compliance, Source Documentation, EDC Systems
Denver, Colorado, United States · On-site
Position: Site Manager (Full-Time/Exempt) The Site Manager is responsible for effectively managing day-to-day site activities for optimization of site performance. The Site Manager is responsible for driving the site to …
Skills: Clinical Research Management, Staff Supervision, Regulatory Compliance, Operational Planning, Quality Control
Midlothian, Virginia, United States · On-site
Position: Site Manager (Full-Time/Exempt) The Site Manager is responsible for effectively managing day-to-day site activities for optimization of site performance. The Site Manager is responsible for driving the site to …
Skills: Clinical Research Management, Staff Supervision, Regulatory Compliance, Operational Planning, Quality Control
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The Psychometric Rater conducts clinical interviews and rating scales for research participants across various health conditions in compliance with FDA and GCP regulations. They are also responsible for maintaining source documentation, ensuring subject safety, and collaborating with sponsors and monitors.
A Master's degree in a related field is required, with a PhD strongly preferred and at least one year of experience in psychometric rating. Proficiency in specific rating scales (e.g., SCID-5-CT, MADRS, PANSS) and the ability to travel up to 70% are highly desired.
Position: Psychometric Rater (Full-Time/Exempt)
The Psychometric Rater will be responsible for interviewing research participants and their informants/caregivers, who are being evaluated to participate in a research study for various health conditions, in compliance with study protocol, SOPs, GCP, ICH, and FDA Regulations.
Reports to: Chief Development Officer
Job Description:
Required Skills/Abilities:
Education and Experience:
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Proven Sites. Engaged Physicians. Predictable Performance.
Founded in 2006, Tekton Research is a multi-specialty clinical research site organization conducting Phase 1–4 clinical trials across neurology and psychiatry, cardiometabolic medicine, general medicine, infectious disease, and pediatrics. Tekton works with Sponsors, CROs, and emerging biotech companies to support practical, well-run clinical trials from startup through enrollment, retention, and closeout. The Tekton model combines experienced investigators, engaged clinical staff, centralized operations, and a commitment to participant-centered care. With performant sites and therapeutic depth across multiple specialties, Tekton helps clients execute complex studies with the operational discipline, extensive patient access, and site-level accountability needed to simplify complex and high-volume trials. Learn more at tektonresearch.com.
Offices: 4534 West Gate Blvd #110, Austin, Texas 78745, US · 19016 Stone Oak Pkwy, Suite 240, San Antonio, Texas 78258, US
Proven Sites. Engaged Physicians. Predictable Performance.
Founded in 2006, Tekton Research is a multi-specialty clinical research site organization conducting Phase 1–4 clinical trials across neurology and psychiatry, cardiometabolic medicine, general medicine, infectious disease, and pediatrics. Tekton works with Sponsors, CROs, and emerging biotech companies to support practical, well-run clinical trials from startup through enrollment, retention, and closeout. The Tekton model combines experienced investigators, engaged clinical staff, centralized operations, and a commitment to participant-centered care. With performant sites and therapeutic depth across multiple specialties, Tekton helps clients execute complex studies with the operational discipline, extensive patient access, and site-level accountability needed to simplify complex and high-volume trials. Learn more at tektonresearch.com.
Offices: 4534 West Gate Blvd #110, Austin, Texas 78745, US · 19016 Stone Oak Pkwy, Suite 240, San Antonio, Texas 78258, US
