Remote Centralized Monitoring Analyst (CMA) – SAS Expert

Insud Pharma; Málaga; Remote; EUR 65,000 - 100,000; Full time

Job summary

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role. You will support the centralized monitoring process by programming QTLs, KRIs, and data quality assessments, and refresh the CM platform to identify signals.

Strong SAS skills and Cluepoints experience are essential, as is the ability to work autonomously and communicate with global teams. You will contribute to study CMP execution, maintain CM specifications, and ensure data confidentiality.

Qualifications

• At least 3 years in pharmaceutical R&D or related field, preferably centralized Monitoring, data management, or biostatistics.
• Experience with Cluepoints is preferred.
• Excellent communication, interpersonal, organizational and problem-solving skills.
• High initiative and ability to work with limited supervision.
• Knowledge of GCP/Good Clinical Data Management Practices is a plus.

Responsibilities

• Support the Centralized Monitoring Lead in developing CM strategy for the study.
• Set up and program QTL, KRI, and Data Quality Assessments per CMP.
• Refresh Centralized Monitoring Platform at defined frequency to identify signals.
• Generate and maintain CM platform specifications and file in eTMF.
• Review protocol thoroughly and understand data sources and transfer specs.
• Coordinate with CM platform setup by peers and document peer reviews.
• Communicate with stakeholders locally and globally.

Skills

SAS programming

Cluepoints

Communication

Organisation

Problem-solving

Data confidentiality

Stakeholder engagement

Tools

Relational databases

EDC systems

Job description

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role. You will support the centralized monitoring process by programming QTLs, KRIs, and data quality assessments, and refresh the CM platform to identify signals.

Strong SAS skills and Cluepoints experience are essential, as is the ability to work autonomously and communicate with global teams. You will contribute to study CMP execution, maintain CM specifications, and ensure data confidentiality.