Remote BPD Clinical Trial Rater - Part-Time Expert

IQVIA; Chicago (IL); Remote; USD 55,000 - 83,000; Part time

Benefits offered by this job

Remote work available

Job summary

IQVIA seeks an experienced Clinical Trial Rater to support a Borderline Personality Disorder study. The role involves conducting structured interviews and administering validated scales with emphasis on data quality and objectivity.

The position is remote-based in the United States, part-time (approximately 5 hours per week) with immediate start and contract-based terms. You will work with investigators and sponsor teams while maintaining GCP standards.

Qualifications

• PhD or PsyD, MD or DO or equivalent licensed clinician.
• Minimum 3 years clinical experience with BPD.
• Minimum 3 years as clinical trial rater with semi-structured assessments.
• Experience using CGI-S/CGIC CGI-C scales.

Responsibilities

• Conduct structured and semi-structured clinical interviews with trial participants diagnosed with BPD.
• Administer, score, and document validated psychiatric rating scales (CGI-S, CGIC/CGIC-S).
• Maintain inter-rater reliability; participate in calibration and quality reviews.
• Identify and escalate safety concerns per protocol and sponsor guidelines.
• Collaborate with investigators, site staff, and sponsor/CRO teams for trial execution.
• Adhere to GCP, SOPs, and ethical guidelines at all times.
• Maintain participant confidentiality with a trauma-informed, empathetic approach.

Skills

Structured interviews

Interviewing skills

Inter-rater reliability

Safety assessment

Team collaboration

Regulatory compliance

Education

PhD or PsyD

MD/DO/FMD

Licensed Clinician

Job description

IQVIA seeks an experienced Clinical Trial Rater to support a Borderline Personality Disorder study. The role involves conducting structured interviews and administering validated scales with emphasis on data quality and objectivity.

The position is remote-based in the United States, part-time (approximately 5 hours per week) with immediate start and contract-based terms. You will work with investigators and sponsor teams while maintaining GCP standards.