Clinical Independent Rater - Romanian Speaking
Location: Remote/Virtual
Estimated 10–16 hours per month
Role: Clinical Independent Rater for Clinical Trials
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.
The CIR plays a key role in ensuring the integrity and reliability of clinical trial data. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., Additional tasks may include assisting with communication materials and documentation.
Participate in all required orientation, training,



and calibration activities.
Review case data and prepare for rater discussions, ensuring all relevant documents and assessment materials are available.
Provide feedback and guidance to raters on assessment methodology, interview techniques, and scoring accuracy through live interactions.
Complete assigned assessments, rater interactions, and related activities according to study timelines and schedules.
Work directly with study participants while maintaining protocol compliance and data quality standards.
Submit all required documentation, reports, and assessment records accurately and within required timelines.
Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred.
Experience:
Minimum 3 years of clinical trial experience with psychiatric populations.
Minimum 3 years administering scales in clinical research trials (excluding graduate/do

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