Clinical Research Psychometric Rater

Tekton Research is seeking an experienced clinical research Psychometric Rater to join our team in Houston, Texas.

About the role

The Psychometric Rater will interview research participants and their informants/caregivers, evaluating eligibility for research studies across various health conditions while ensuring compliance with study protocols, SOPs, GCP, ICH, and FDA regulations.

Responsibilities

• Review subjects' medical history and conduct prescreening interviews to assess eligibility for specific studies.
• Administer psychometric rating scales for subjects with diagnoses such as ADHD, Alzheimer’s Disease, Bipolar Disorder, GAD, Major Depressive Disorder, PTSD, Substance Use Disorders, Epilepsy, Anxiety Disorders, and Schizophrenia/Schizoaffective Disorder, adhering to study protocols and regulatory guidelines.
• Travel to other Tekton sites to conduct ratings as needed (up to 50-70% travel).
• Ensure subject safety by responding appropriately to any identified risks of harm to self or others.
• Collaborate with site staff and business development to promote Tekton’s services to sponsors and CROs.
• Attend and present at conferences when required.
• Calculate and interpret rating scale results to determine protocol eligibility.
• Meet with sponsors, study monitors, and medical monitors to address questions about ratings.
• Maintain consistency in rating performance and review ratings across studies for efficacy.
• Maintain source documentation per ALCOA-C standards and resolve monitor/sponsor queries.
• Complete sponsor-assigned training and meetings to obtain and maintain rater certification.
• Attend company training programs, webinars, and study meetings as required.
• Maintain confidentiality of subjects, customers, and company information.
• Perform other duties as assigned.

Requirements

• Master’s degree in a related field (PhD strongly preferred).
• 1+ years’ experience performing psychometric rating scales in a clinical setting or clinical trials, or equivalent education/experience.
• Current or previous certifications for scales such as 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 are highly preferred.
• Bilingual (English/Spanish) proficiency is a plus.
• Experience as a Clinical Research Coordinator is a plus.

Skills

• Proficiency with Microsoft applications, email, electronic health records, and web applications.
• Typing proficiency (40+ WPM).
• Strong organizational skills and attention to detail.
• Excellent written and verbal communication skills.
• Strong interpersonal and listening skills; ability to work independently and collaboratively.
• Ability to manage multiple tasks and adapt to changing priorities.
• Professional, respectful, self-motivated, and strong work ethic.
• High integrity, dependability, and ability to work with minimal supervision.
• Problem-solving skills and ability to handle sensitive information.

Physical Requirements

• Prolonged periods of sitting at a desk and working on a computer.
• Ability to lift up to 15 pounds at times.