Psychometric Rater - Permanent - Englewood, NJ
Are you looking to drive groundbreaking clinical research and make a real impact? Join our client and lead the way in advancing clinical trials!
Proclinical is seeking a Psychometric Rater to support clinical trials by conducting structured interviews and administering standardized rating scales to study participants.
Primary Responsibilities:
In this role, you will play a vital part in evaluating psychiatric and neurological conditions while ensuring assessments align with clinical trial protocols and regulatory standards. This position is ideal for individuals with a background in psychology, neuroscience, behavioural health, or clinical research who have hands-on experience with psychometric rating scales.
Skills & Requirements:
- Bachelor's degree in Psychology, Neuroscience, Clinical Research, Behavioral Health, or a related field.
- Hands-on experience administering psychometric rating scales in a clinical or research setting.
- Familiarity with clinical trials or research site operations is preferred.
- Strong interviewing and assessment skills, particularly 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 environment.
- Strong communication and interpersonal skills when working with patients, caregivers, and study teams.
- Experience or certification in administering assessments such as SCID-5-CT, MINI, MADRS, HAM-A, HAM-D, PANSS, C-SSRS, YMRS, MMSE, MOCA, ADAS-Cog, CGI, HDRS-17, RBANS, CDR, LSAS is highly preferred.
- Bilingual English-Spanish is a plus.
The Psychometric Rater's responsibilities will be:
- 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 consistency and quality in ratings across 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.
Compensation:
- $90,000 to $110,000 per annum.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
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