Clinical Trial Rater

IQVIA • Durham, NC

3d • Remote

About The Position

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We collaborate with top pharmaceutical and biotech companies to accelerate innovation and improve patient outcomes. Our mission is to combine data science and human expertise to transform healthcare worldwide. We are seeking experienced and reliable Clinical Trial Raters to conduct standardized psychiatric assessments for a clinical trial in Borderline Personality Disorder (BPD). The rater will be responsible for administering validated clinician‑rated instruments, ensuring high-quality, consistent data collection in accordance with the study protocol, GCP, and regulatory requirements. This role requires strong clinical judgment, experience with psychiatric populations, and the ability to maintain objectivity and inter‑rater reliability across multiple assessments and time points.

Requirements

• Advanced degree in a relevant field (e.g. Psychology, Psychiatry or related discipline)
• At least 3 years clinical experience working with Borderline Personality Disorder patients
• Experience as clinical trial rater or assessor in CNS trials
• Demonstrated experience with clinician‑rated psychiatric scales
• Strong interviewing skills with the ability to manage emotionally complex or sensitive interactions
• Excellent attention to detail and documentation skills

Responsibilities

• Conduct structured and semi‑structured clinical interviews with trial participants diagnosed with Borderline Personality Disorder
• Administer, score, and document validated psychiatric rating scales: Zanarini Rating Scale for Borderline Personality Disorder (ZAN‑BPD) and McLean Screening Instrument for BPD (MSI‑BPD)
• Maintain inter‑rater reliability, including participation in calibration, training, and quality review sessions
• Identify and escalate safety concerns (e.g. suicidality) according to protocol and sponsor guidelines
• Work closely with study investigators, site staff, and sponsor/CRO teams to support high‑quality trial execution
• Adhere to Good Clinical Practice (GCP), SOPs, and ethical guidelines at all times
• Maintain participant confidentiality and a trauma‑informed, empathetic approach during all assessments

Benefits

• Flexible, remote work schedule.
• Opportunity to contribute to global clinical research.
• Collaborate with a team committed to improving patient care and advancing science

What This Job Offers

• Job Type: Part-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree
• Number of Employees: 5,001-10,000 employees