CMA: Centralized Monitoring Analyst — SAS & Cluepoints

Mediclinic; Polokwane; Remote; ZAR 700.000 - 900.000; Vollzeit

Zusammenfassung

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) to remotely manage centralized monitoring activities within sponsor projects. The role emphasizes SAS programming expertise, data management, and strong communication across global teams.

You will support CM strategy development, configure QTLs and KRIs, and refresh CM platforms to identify signals. A thorough understanding of studies, data flows, and regulatory requirements is required.

Qualifikationen

• 3+ years 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.
• Ability to work autonomously and engage with stakeholders to execute study-level CM processes.
• Understanding of data sources, data transfer specifications and data structure.
• Experience with relational databases, Clinical Data Management and EDC Systems.
• Excellent command of English, both written and verbal.

Aufgaben

• Supports the Centralized Monitoring Lead (CML) in developing a fit-for-purpose CM strategy by identifying CM elements for the study (QTLs, KRIs, data visualizations, Data Quality Assessments).
• Set up/Program QTL, KRI and Data Quality Assessments per 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 the protocol is key.
• Understand data sources, data transfer specifications, and data structure.
• Execute and document peer-review of CM platform setup done by other CMA colleagues.

Kenntnisse

SAS programming

Cluepoints

Centralized Monitoring

Communication

Data Management

EDC Systems

Biostatistics

Tools

SAS Macro language

Jobbeschreibung

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) to remotely manage centralized monitoring activities within sponsor projects. The role emphasizes SAS programming expertise, data management, and strong communication across global teams.

You will support CM strategy development, configure QTLs and KRIs, and refresh CM platforms to identify signals. A thorough understanding of studies, data flows, and regulatory requirements is required.