PRN Psychometric Rater/Clinical Rater

About this role

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion. Join a Leading Clinical Research Organization Advancing Neurology & Psychiatry Treatments Caribbean Medical Research Center (CMRC), a wholly owned subsidiary of Headlands Research, is a premier clinical research company specializing in Neurology, Psychiatry, Internal Medicine, and Women’s Health, that is seeking a Clinical Rater (RN, Psychometrist, or Psychometrician) to conduct cognitive and psychometric assessments for groundbreaking Alzheimer’s, Mild Cognitive Impairment, Depression, Anxiety, and Parkinson’s Disease clinical trials.

As part of Headlands Research, a fast-growing network of cutting-edge clinical trial sites, we are committed to improving patient outcomes and advancing medical breakthroughs through innovative research and technology. We are currently seeking a Part-time (one 8-hour day per week or two 4-hour days per week) experienced Clinical Rater or Psychometrician to perform neurocognitive and psychiatric assessments for adult and geriatric populations in FDA-regulated trials.

The ideal candidate has experience administering standardized neurocognitive and psychiatric rating scales such as CDR (Clinical Dementia Rating) and PACC-5 (Preclinical Alzheimer’s Cognitive Composite 5). 📍 Location: San Juan, PR (Onsite – No Remote Work) ⏰ Clinic Hours: Mondays through Fridays, 8:00 AM – 5:00 PM 💲 Pay: Based upon relevant experience, certifications, and education. 🚗 Travel Required: No Responsibilities: Administer and score study-specific standardized clinical scales and psychometric tests to evaluate cognitive function, disease severity/progression, and study eligibility.

Conduct in-person cognitive, diagnostic, and clinical assessments with study participants and caregivers following protocols, GCP, and FDA regulations. Maintain consistency in rating performance over time to ensure accuracy and prevent rater drift. Communicate assessment findings with lead physicians, study sponsors, CROs, and internal teams. Maintain accurate and timely documentation for all assessments and study-related activities.