Remote Centralized Monitoring Analyst (CMA) - SAS Pro

Reteitalianalca; Barcelona; À distance; EUR 55 000 - 75 000; Plein temps

Résumé du poste

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role. As a CMA lead programmer on Cluepoints, you will configure, program and refresh the Centralized Monitoring platform per CMP, and work with client teams to deliver study-level monitoring.

Requirements include 3+ years in pharma R&D with centralized monitoring, 2–3 years SAS with macro language, and knowledge of Cluepoints. Strong communication and organizational skills are essential for global collaboration.

Qualifications

• Minimum 3 years in pharma R&D or related field, with centralized monitoring, data management or biostatistics.
• 2–3 years SAS experience including macro language.
• Knowledge/experience working on Cluepoints and central monitoring systems.

Responsabilités

• Supports the Centralized Monitoring Lead in developing CM strategy and CM elements (QTL, KRI, data visualizations).
• Set up/program QTL, KRI and Data Quality Assessments per CMP.
• Refresh CM platform at defined frequency to enable signal identification.
• Generate and maintain CM platform specifications document and file in eTMF.
• Review study protocol and understand data sources and transfer specs.
• Execute peer-review of CM platform setup by CMA colleagues.

Connaissances

SAS programming

Communication

Organisation

Cluepoints familiarity

Outils

Cluepoints

Description du poste

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role. As a CMA lead programmer on Cluepoints, you will configure, program and refresh the Centralized Monitoring platform per CMP, and work with client teams to deliver study-level monitoring.

Requirements include 3+ years in pharma R&D with centralized monitoring, 2–3 years SAS with macro language, and knowledge of Cluepoints. Strong communication and organizational skills are essential for global collaboration.