Remote Centralized Monitoring Lead - SAS & Cluepoints

Blu; Barcelona; A distancia; EUR 53.000 - 88.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote position. The role focuses on setting up and refreshing the Centralized Monitoring platform, programming QTLs and KRIs, and ensuring data quality across study CMPs. Strong SAS skills and Cluepoints experience are required.

Responsibilities include collaborating with CM leads, validating protocols, and maintaining CM documentation while communicating with stakeholders globally. English proficiency is essential.

Formación

• At least 3 years relevant experience in pharmaceutical R&D or related field, preferably centralized monitoring, data management, and/or biostatistics.
• 2-3 years SAS experience including macro language.
• Knowledge/ experience working on Cluepoints.
• Ability to work autonomously and engage with relevant stakeholders to execute activities related to study level centralized monitoring process.
• Ability to understand basic statistical analysis concepts and to interpret their outcome.
• Ability to maintain confidentiality of data and information during interactions with staff at all levels.
• Experience with relational databases, preferably Clinical Data Management and EDC Systems.
• Excellent command, both verbal and written, of English.

Responsabilidades

• Supports the Centralized Monitoring Lead in the development of the fit-for purpose CM strategy by contributing to the identification of the relevant CM elements to be implemented for the study (Quality Tolerance Limits, Key Risk Indicators, data visualizations and Data Quality Assessments).
• Setup/Program QTL, KRI and Data Quality Assessments according to the study CMP.
• Refresh the Centralized Monitoring Platform at predefined frequency to enable signal identification.
• Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF.
• Review and understanding of protocol is key.
• Understand the data sources for the study, the data transfer specifications and the data structure.
• Execute and document peer-review of CM platform setup done by other CMA colleagues.

Conocimientos

SAS programming

Autonomous work

Communication skills

Stakeholder engagement

Cluepoints knowledge

Data management

Biostatistics

Herramientas

Cluepoints

Relational databases

EDC Systems

Descripción del empleo

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote position. The role focuses on setting up and refreshing the Centralized Monitoring platform, programming QTLs and KRIs, and ensuring data quality across study CMPs. Strong SAS skills and Cluepoints experience are required.

Responsibilities include collaborating with CM leads, validating protocols, and maintaining CM documentation while communicating with stakeholders globally. English proficiency is essential.