Clinical Independent Rater
Pubblicato il 06-10-2026 - Medicina in Bardi
Clinical Independent Rater - Romanian Speaking
Massimizzi le sue possibilità di successo assicurandosi che il suo CV e le sue competenze corrispondano ai requisiti di questa posizione.
Location:
Remote/Virtual
Hours: 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.
Position Overview
The CIR plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. 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., mock interviews). Additional tasks may include assisting with communication materials and documentation.
Key Responsibilities
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.
Conduct patient interviews and clinical assessments with study participants.
Administer, score, and interpret clinical rating scales and structured interviews.
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 m