Clinical Trial Psychologist

We are seeking a detail-oriented and reliable Clinical Trial Psychologist to join our clinical research team in a dedicated rater role. The successful candidate will be responsible for administering, scoring, and documenting standardized clinical rating scales in accordance with clinical trial protocols, assessment manuals, and applicable Good Clinical Practice (GCP) requirements.

The role will focus primarily on the assessment of participants in clinical trials involving psychiatric and psychological conditions, with particular emphasis on the Montgomery–Åsberg Depression Rating Scale (MADRS) and other study-specific clinical outcome assessments.

The postholder will ensure accurate, consistent, and objective ratings, maintain appropriate inter-rater reliability, and contribute to the quality and integrity of clinical trial data. The role does not involve independent diagnosis, treatment, or clinical management of participants.

Key Responsibilities

• Administer and score the MADRS and other protocol-specified psychological or psychiatric rating scales in accordance with standardized assessment procedures.

• Conduct structured or semi-structured clinical interviews as required by the relevant rating instruments and study protocols.

• Complete assessments at scheduled study visits and within protocol-defined visit windows.

• Maintain consistency, objectivity, and reliability in scoring, minimizing assessment bias and inter-rater variability.

• Complete all required scale-specific training, certification, and calibration exercises before conducting assessments, where applicable.

• Accurately document ratings, assessment findings, and relevant observations in source documents and electronic data capture systems, as required.

• Ensure that all assessments are completed in accordance with the approved protocol, assessment manuals, and study-specific instructions.

• Identify and promptly report missing information, scoring discrepancies, and data inconsistencies to the appropriate study team members.

• Maintain up-to-date training records and comply with study-specific requirements for rater qualification and ongoing competency.

• Communicate any clinically significant observations, deterioration in mental state, or potential participant safety concerns to the Principal Investigator or designated clinician in accordance with site procedures.

• Maintain participant confidentiality and adhere to applicable data protection requirements, research ethics, and GCP standards.

• Collaborate with the Principal Investigator, Clinical Research Coordinators, and other site personnel to support the timely and accurate completion of clinical assessments.