Remote Centralized Monitoring Analyst (Cluepoints & SAS)

Manpowergroup Eña; Madrid; Remote; EUR 65,000 - 90,000; Full time

Job summary

IQVIA invites applications for a Clinical Monitoring Analyst (Cluepoints) role focused on centralized monitoring in pharmaceutical research. The position requires SAS programming experience and strong communication skills to manage client-facing deliveries for a sponsor-driven project.

The CMA collaborates with the Centralized Monitoring Lead to implement CM strategies, QTLs, KRIs, and data visualizations, while ensuring adherence to regulatory standards and data quality across studies.

Qualifications

• 3+ years of experience in pharmaceutical R&D or related field, preferably centralized Monitoring, data management or biostatistics.
• 2-3 years SAS experience including macro language.
• Knowledge/experience working on Cluepoints.
• Ability to work autonomously and engage with stakeholders on study-level CM processes.
• Understanding of basic statistical concepts and interpretation of results.
• Maintain confidentiality of data across levels of staff.
• Excellent verbal and written English.

Responsibilities

• Support the Centralized Monitoring Lead in developing CM strategy by identifying CM elements for studies (QTL, KRI, data visualizations, DQA).
• Setup and program QTL, KRI, and Data Quality Assessments per study CMP.
• Refresh the Centralized Monitoring Platform at predefined frequencies to enable signal identification.
• Generate and maintain CM platform specifications documentation and file in eTMF.
• Review study protocol and understand data sources, transfer specs, and data structures.
• Document peer-review of CM platform setup performed by CMA colleagues.

Skills

SAS programming

Centralized Monitoring

Scientific/Data analysis

Communication

Stakeholder engagement

Programming concepts

Tools

Cluepoints

Job description

IQVIA invites applications for a Clinical Monitoring Analyst (Cluepoints) role focused on centralized monitoring in pharmaceutical research. The position requires SAS programming experience and strong communication skills to manage client-facing deliveries for a sponsor-driven project.

The CMA collaborates with the Centralized Monitoring Lead to implement CM strategies, QTLs, KRIs, and data visualizations, while ensuring adherence to regulatory standards and data quality across studies.