Remote Centralized Monitoring Lead | SAS & Data Quality

Clarios; Madrid; Remote; EUR 60,000 - 90,000; Full time

Job summary

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) for a remote role to manage centralized monitoring activities. You will work on Cluepoints, programming QTLs and KRIs, and refreshing the CM platform per CMP, with close collaboration across study teams.

Ideal candidates have 3+ years in pharmaceutical research and SAS experience (including macros), strong communication, and ability to work autonomously with stakeholders while ensuring data integrity and regulatory compliance.

Qualifications

• At least 3 years relevant experience 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 with stakeholders to execute study CM processes.
• Strong communication and problem-solving skills.

Responsibilities

• Supports the Centralized Monitoring Lead in developing the fit-for-purpose CM strategy.
• Setup/Program QTL, KRI and Data Quality Assessments per CMP.
• Refresh CM Platform to enable signal identification.
• Document CM platform specifications and file in eTMF.
• Review protocol and data sources to understand data structure.
• Peer-review CM platform setup across CMA colleagues.

Skills

SAS programming

Communication

Organization

Clinical Data Management

Data visualization

Tools

Cluepoints

SAS macro language

Job description

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) for a remote role to manage centralized monitoring activities. You will work on Cluepoints, programming QTLs and KRIs, and refreshing the CM platform per CMP, with close collaboration across study teams.

Ideal candidates have 3+ years in pharmaceutical research and SAS experience (including macros), strong communication, and ability to work autonomously with stakeholders while ensuring data integrity and regulatory compliance.