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About IQVIAIQVIA is a global leader hnology 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 , 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.Key ResponsibilitiesConduct structured and semi‑structured clinical interviews with trial participants diagnosed with Borderline Personality DisorderAdminister, score, and document validated psychiatric rating scales: CGI-S, and CGI-C or CGIC-SMaintain inter‑rater reliability, including participation ining, and quality review sessionsIdentify and escalate safety concerns (e.g. suicidality) according to protocol and sponsor guidelinesWork closely with study investigators, site staff, and sponsor/CRO teams to support high‑quality trial executionAdhere to Good Clinical Practice (GCP), SOPs, and ethical guidelines at all timesMaintain participant confidentiality and a trauma‑informed, empathetic approach during all assessmentsRequired QualificationsEducation: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign Medical Doctor (FMD), or Doctor of Osteopathic Medicine (DO)Licensure: Licensed Clinician: MD/FMD/DO, Psychiatrist, Clinical Psychologist, Psychotherapist, Mental Health Counselor/Practitioner (LMHC/LCMHC/LMHP) or Professional Counselor (LPC/LCPC/LPCC)Clinical Experience: 3 years of clinical experience with Borderline Personality Disorder (BPD) populationClinical Trial Rater Experience 3 years of experience as clinical trial rater, including semi-structured psychiatric assessments3 years of experience with Clinical Global Impression rating scalesClinical Global Impression-Severity (CGI-S) and Clinical Global Impression-Change (CGI-C) or Clinical Global Impression-Change in Severity (CGIC-S)Why Work With Us?Flexible, remote work schedule.Opportunity to contribute to global clinical research.Collaborate with a team committed to improving patient care and advancing science.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
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