Rater- 255852

We are seeking an experienced Psychometric Rater to join a growing clinical research team. This role is ideal for a clinical research professional with strong experience administering and scoring standardized clinical assessments and working directly with study participants.The Psychometric Rater will be responsible for conducting protocol-specific assessments, maintaining accurate documentation, and ensuring assessments are performed consistently and in accordance with study requirements, regulatory guidelines, and Good Clinical Practice (GCP).ResponsibilitiesAdminister standardized psychometric and clinical rating scales in accordance with study protocols.Conduct participant interviews and assessments while maintaining a professional and empathetic approach.Accurately score, document, and enter assessment results into applicable clinical research systems.Ensure assessments are completed within required study timelines and according to protocol.Maintain accurate source documentation and study records.Collaborate with investigators, clinical research coordinators, and other study team members.Identify and appropriately communicate potential protocol deviations, safety concerns, or issues affecting assessment validity.Participate in training and certification for study-specific rating instruments.Maintain compliance with GCP, study protocols, SOPs, and applicable regulatory requirements.Support overall clinical trial operations as needed.QualificationsMinimum 2 years of clinical research experience required.Previous experience administering psychometric, behavioral, psychiatric, neurological, or other clinical rating scales strongly preferred.Experience working directly with clinical trial participants.Strong understanding of clinical research processes and GCP.Excellent attention to detail and ability to follow standardized assessment procedures.Strong interpersonal, communication, and documentation skills.Ability to work independently while collaborating effectively with a multidisciplinary research team.Experience with electronic clinical research systems/EDC platforms is a plus.