Remote Clinical Trial Rater - BPD Specialist (Part-Time)

IQVIA; Springfield (MA); Sur place; USD 7 800 - 12 000; Temps partiel

Résumé du poste

IQVIA is seeking a remote Clinical Trial Rater to conduct standardized psychiatric assessments for a Borderline Personality Disorder study. The role emphasizes accuracy, objectivity, and inter-rater reliability, with adherence to GCP and protocol to ensure high-quality data collection.

Responsibilities include structured interviews, CGI-S/CGIC-S administration, calibration sessions, safety monitoring, and collaboration with investigators and sponsor teams. Immediate start; approx.

Qualifications

• Doctoral or medical degree and licensed clinician.
• 3 years of clinical experience with BPD population.
• 3 years of clinical trial rater experience with CGI-S/CGI-C/CGIC-S.

Responsabilités

• Conduct structured and semi-structured clinical interviews with trial participants diagnosed with Borderline Personality Disorder.
• Administer, score, and document validated psychiatric rating scales: CGI-S, and CGI-C or CGIC-S.
• Maintain inter-rater reliability, including calibration, training, and quality review sessions.
• Identify and elevate safety concerns 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.

Connaissances

Clinical assessment

Inter-rater reliability

Safety monitoring

CGI scales administration

Formation

PhD/PsyD/MD/DO

Description du poste

IQVIA is seeking a remote Clinical Trial Rater to conduct standardized psychiatric assessments for a Borderline Personality Disorder study. The role emphasizes accuracy, objectivity, and inter-rater reliability, with adherence to GCP and protocol to ensure high-quality data collection.

Responsibilities include structured interviews, CGI-S/CGIC-S administration, calibration sessions, safety monitoring, and collaboration with investigators and sponsor teams. Immediate start; approx.