Rater

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).

Responsibilities

• Administer 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.

Qualifications

• Minimum 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.