Clinical Independent Rater
5 giorni fa
Conscenti Ne Liguria, Ne (GE); Provincia di Genova; Liguria, Italia
IQVIA Argentina
Tempo pieno
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Clinical Independent Rater
- Romanian Speaking Le seguenti informazioni hanno lo scopo di fornire ai potenziali candidati una migliore comprensione dei requisiti per questo ruolo. Remote/Virtual Estimated 10–16 hours per month 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/doctoral research). Experience in CNS trials preferred. Strong interpersonal and communication skills for professional interaction at all levels. Proficiency with Windows and Microsoft Office applications. Language Requirement Current openings require fluency in English and native-level proficiency in Romanian(Moldova). #LI-DNP #LI-Remote #LI-HCPN 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. xrdztoy Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
- Romanian Speaking Le seguenti informazioni hanno lo scopo di fornire ai potenziali candidati una migliore comprensione dei requisiti per questo ruolo. Remote/Virtual Estimated 10–16 hours per month 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/doctoral research). Experience in CNS trials preferred. Strong interpersonal and communication skills for professional interaction at all levels. Proficiency with Windows and Microsoft Office applications. Language Requirement Current openings require fluency in English and native-level proficiency in Romanian(Moldova). #LI-DNP #LI-Remote #LI-HCPN 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. xrdztoy Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.