Clinical Research Psychometric Rater

Tekton Research; Houston (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

Tekton Research in Houston, TX is seeking an experienced Psychometric Rater to interview participants and informants for clinical studies, ensuring alignment with study protocols, GCP, ICH, and FDA regulations.

The role requires administering a range of rating scales across multiple conditions, travel to Tekton sites when needed, maintaining ALCOA-C source documentation, and collaborating with sponsors and monitors.

Qualifications

• Master's degree required; PhD preferred.
• 1+ years' experience performing psychometric rating scales in clinical settings or trials.
• Certifications to rate scales (SCID-5-CT, MINI, LSAS, HAM-A/D, etc.) preferred.

Responsibilities

• Interview research participants and informants per study protocol.
• Administer psychometric rating scales across diagnoses.
• Travel to Tekton sites to conduct ratings as needed.
• Ensure participant safety and respond to potential harm.
• Maintain ALCOA-C source documentation; respond to sponsor queries.
• Collaborate with sponsors, monitors, and site staff; attend conferences as needed.

Skills

General computer skills

Organizational skills

Written and verbal communication

Interpersonal and listening skills

Multitasking and adaptability

Professional conduct and integrity

Independent work capability

Data privacy and confidentiality

Education

Master's degree in related field

PhD preferred

Certifications in rating scales (SCID-5-CT, MINI, LSAS, HAM-A/D, etc.)

Tools

EHR systems

Job description

Tekton Researchis looking for an experienced clinical research Psychometric Rater in Houston, Texas to join our team!

Position: Psychometric Rater (Full-Part/Exempt/On-Site)

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:

• Reviewing the subject's medical history, meeting with potential subjects, collecting information through a prescreening interview and discussing with the Study team criteria for eligibility for a particular study.
• Conducting a variety of psychometric rating scales on subjects with various diagnoses (such as ADHD, Alzheimer's Disease, Bipolar Disorder, GAD, Major Depressive Disorder, Post Traumatic Stress Disorder, Substance Use Disorders, Epilepsy, Anxiety Disorders, and Schizophrenia/Schizoaffective Disorder) for our clinical trials, in compliance with specific study protocols, FDA, GCP, ICH, and privacy guidelines.
• Ability and willingness to travel to other Tekton sites to conduct ratings when needed.
• Ensuring the subject's safety by responding appropriately to any potential for harm to self or others that are identified through the evaluations performed.
• Working closely with other site staff and business development to promote Tekton and our sites to sponsors and CROs for new studies.
• Attendance and presentations at conferences when needed.
• Calculating and utilizing rating scale results as appropriate to determine protocol eligibility.
• Meet with Sponsors, Study Monitors, and Medical Monitors as needed to address questions regarding ratings.
• Working diligently to maintain consistency in the performance of ratings. Reviewing ratings across studies and subjects to ensure efficacy and consistency.
• Maintaining source documentation in accordance with ALCOA-C standards and completing all monitor and sponsor queries.
• Completing all sponsor-assigned training and meetings to obtain rater certification and re-certification per protocols requirements.
• Attending and successfully completing all company training programs; participating in webinars and other study meetings as needed.
• Maintaining confidentiality of subjects, customers, and company information.
• Other duties as requested or assigned.

Required Skills/Abilities:

• Proficiency with computer applications such as Microsoft applications, email, electronic health records, and web applications, and the ability to type proficiently (40+ wpm).
• Strong organizational skills and attention to detail.
• Well-developed written and verbal communication skills.
• Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers, and external customers.
• Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
• Must be professional, respectful of others, self-motivated, and have a strong work ethic.
• Must possess a high degree of integrity and dependability.
• Ability to work under minimal supervision, identify problems and implement solutions.
• Ability to handle highly sensitive information

Education and Experience:

• Master's degree in a related field required, 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