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Psychometric Rater

Proclinical St. Louis 10.11.2026 Déposer ma candidature
Empresa
Proclinical
Lugar
St. Louis
Fecha
10.11.2026
Referencia
383863

Shape the Future of Psychiatric and Neurological Treatments

Are you passionate about mental health research and skilled in administering clinical assessments? Join a team dedicated to supporting clinical trials by conducting structured interviews and administering standardized rating scales to study participants. In this role, you will play a key part in evaluating psychiatric and neurological conditions while ensuring all assessments are completed in strict accordance with clinical trial protocols and regulatory standards.

Primary Responsibilities

  • Conduct clinical interviews and prescreening assessments to evaluate participant eligibility for clinical trials.
  • Administer standardized psychometric rating scales to participants with conditions such as Major Depressive Disorder, Bipolar Disorder, Schizophrenia, PTSD, ADHD, Alzheimer's Disease, Anxiety Disorders, and Substance Use Disorders.
  • Score and interpret assessments to determine protocol eligibility and study compliance.
  • Maintain high consistency and quality in ratings across multiple studies.
  • Collaborate with clinical research teams, sponsors, and study monitors to address assessment-related questions.
  • Ensure participant safety, including identifying and responding to any risk of harm during evaluations.
  • Maintain accurate clinical documentation in compliance with GCP, FDA regulations, and ALCOA-C standards.
  • Complete sponsor training and maintain rater certifications required for clinical studies.
  • Travel to other research sites as needed to conduct assessments.

Education and Experience

  • Bachelor's degree in Psychology, Neuroscience, Clinical Research, Behavioral Health, or a related field.
  • 1+ years of experience administering psychometric rating scales in a clinical or research setting.
  • Experience working in clinical trials or at a research site is preferred.
  • Previous experience as a Clinical Research Coordinator (CRC) is a plus.
  • Bilingual (English/Spanish) is a plus.

Highly Preferred Rating Scale Experience

Candidates with experience or certification administering the following assessments are strongly encouraged to apply:

  • SCID-5-CT
  • MINI
  • MADRS
  • HAM-A / HAM-D
  • PANSS
  • C-SSRS
  • YMRS
  • MMSE
  • MOCA
  • ADAS-Cog
  • CGI-H
  • DRS-17
  • RBA
  • NSCD
  • RLSAS

Key Skills

  • Strong interviewing and assessment skills.
  • Experience working with psychiatric or neurological patient populations.
  • Knowledge of GCP, FDA regulations, and clinical trial procedures.
  • Excellent documentation and organizational skills.
  • Ability to manage multiple studies and priorities in a fast-paced research environment.
  • Strong communication and interpersonal skills when working with patients, caregivers, and study teams.

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