Centralized Monitoring Analyst (CMA) — SAS Programmer Lead

Serveo

Madrid

À distance

EUR 65 000 - 90 000

Plein temps

Il y a 3 jours

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Résumé du poste

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) for a fully remote role across multiple international locations. The CMA will manage centralized monitoring setup, programming and refreshes to support study CMPs, collaborating with the CM Lead and client teams.

Ideal candidates have 3+ years in pharma R&D or related areas, SAS programming (macro language), and experience with Cluepoints. Strong communication and data management skills are essential for success in this sponsor-driven

Qualifications

At least 3 years relevant experience in pharmaceutical research and development or related field, preferably centralized monitoring, data management, and/or biostatistics.
2-3 years SAS experience including macro language.
Knowledge/experience working on Cluepoints.

Responsabilités

Supports the Centralized Monitoring Lead (CML) in developing fit-for-purpose CM strategy by identifying relevant CM elements to implement.
Setup/Program QTL, KRI and Data Quality Assessments according to 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.