Remote Centralized Monitoring Analyst (SAS & Cluepoints)

Marketplace

Sevilla

Remote

EUR 60,000 - 90,000

Full time

7 days ago
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Job summary

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a Remote role in a sponsor-driven project. The CMA will collaborate with the Centralized Monitoring Lead to implement CM elements, including QTLs and KRIs, while ensuring data quality and regulatory compliance.

Strong SAS skills and Cluepoints experience are essential for successful client deliveries. Responsibilities include setting up QTL/KRI, refreshing CM platform, maintaining CMP documents, and peer-review of CM setups.

Qualifications

  • Minimum 3 years in pharmaceutical R&D or centralized monitoring.
  • Experience with SAS programming including macro language is required.
  • Knowledge of Cluepoints and data management practices is essential.

Responsibilities

  • Setup/Program QTL, KRI and Data Quality Assessments according to 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 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.

Skills

SAS programming
Data management
Cluepoints knowledge
Communication skills
Statistical concepts

Tools

Cluepoints platform
Relational databases
EDC systems

Job description

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a Remote role in a sponsor-driven project. The CMA will collaborate with the Centralized Monitoring Lead to implement CM elements, including QTLs and KRIs, while ensuring data quality and regulatory compliance.

Strong SAS skills and Cluepoints experience are essential for successful client deliveries. Responsibilities include setting up QTL/KRI, refreshing CM platform, maintaining CMP documents, and peer-review of CM setups.

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