Remote Centralized Monitoring Analyst (SAS)

GCO Ventures; Barcelona; Remote; EUR 80,000 - 116,000; Full time

Job summary

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) for a remote role. You will support the Centralized Monitoring process, perform CM platform setup, programming and refreshes per CMP, and collaborate with sponsor clients on deliveries.

Ideal candidates have 3+ years in pharma R&D or data management, 2–3 years SAS (including macros), knowledge of Cluepoints, and strong communication with global stakeholders; English fluency is required.

Qualifications

• At least 3 years relevant experience in pharmaceutical research and development or related field preferably in 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 activities related to study level centralized monitoring process.
• Excellent command of English (verbal and written).

Responsibilities

• Supports the Centralized Monitoring Lead (CML) in developing the CM strategy by identifying the relevant CM elements 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 CM platform specifications document and file in eTMF.
• Understand the study protocol and data sources; transfer specs and data structure.
• Execute and document peer-review of CM platform setup done by CMA colleagues.

Skills

SAS programming

Cluepoints experience

Data management

Tools

SAS macro language

Relational databases

EDC systems

Job description

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) for a remote role. You will support the Centralized Monitoring process, perform CM platform setup, programming and refreshes per CMP, and collaborate with sponsor clients on deliveries.

Ideal candidates have 3+ years in pharma R&D or data management, 2–3 years SAS (including macros), knowledge of Cluepoints, and strong communication with global stakeholders; English fluency is required.