Remote Centralized Monitoring Analyst — SAS & Cluepoints

Acercanza Consulting; Boadilla del Monte; A distancia; EUR 42.000 - 64.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Clinical Monitoring Analyst (CMA) for a remote, sponsor-dedicated project. You will support the Centralized Monitoring Lead by configuring CM elements, programming QTLs and KRIs, and refreshing the CM platform per CMP. Strong SAS experience and familiarity with Cluepoints are essential.

You will engage with stakeholders across global teams, review study protocols, and ensure compliant CM setup with high quality documentation and data integrity.

Formación

• 3+ years of relevant pharmaceutical research experience.
• 2-3 years SAS experience including macro language.
• Knowledge/experience with Cluepoints.
• Ability to work autonomously and engage with stakeholders to execute CM activities.
• Strong communication and organizational skills.
• Experience with relational databases and EDC systems.

Responsabilidades

• Supports the Centralized Monitoring Lead in the development of the fit-for purpose CM strategy for the study (QTL, KRI, data visualizations, and Data Quality Assessments).
• Setup/Program QTL, KRI and Data Quality Assessments according to the 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.
• Understand the protocol and data sources, data transfer specs, and data structure.
• Execute and document peer-review of CM platform setup done by CMA colleagues.

Conocimientos

SAS programming

Cluepoints

Data management

Biostatistics

Communication skills

English (fluent)

Herramientas

Relational databases

EDC systems

Descripción del empleo

IQVIA is seeking a Clinical Monitoring Analyst (CMA) for a remote, sponsor-dedicated project. You will support the Centralized Monitoring Lead by configuring CM elements, programming QTLs and KRIs, and refreshing the CM platform per CMP. Strong SAS experience and familiarity with Cluepoints are essential.

You will engage with stakeholders across global teams, review study protocols, and ensure compliant CM setup with high quality documentation and data integrity.