Junior Centralized Monitoring Analyst - SAS (Remote)

Mediaplus Equmedia; Madrid; Remote; EUR 65,000 - 90,000; Full time

Job summary

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role. The CMA will support centralized monitoring activities, set up QTLs/KRIs, and refresh CM platforms according to CMPs, while coordinating with clinical teams and stakeholders.

The role requires SAS programming expertise, knowledge of Cluepoints, and strong communication and organizational skills to ensure compliant, quality data-driven monitoring across studies.

Qualifications

• Minimum 3 years of relevant experience in pharmaceutical R&D or related field (centralized monitoring, data management or biostatistics).
• 2–3 years SAS experience including macro language.
• Knowledge or experience working with Cluepoints.
• Ability to work autonomously and engage with stakeholders to execute study-level CM processes.
• Ability to understand basic statistical concepts and interpret results.
• Maintain confidentiality of data and information across all levels.

Responsibilities

• Support the Centralized Monitoring Lead in developing CM strategy for the study, identifying CM elements to implement (QTLs, KRIs, data visualizations, data quality assessments).
• Set up and program QTL, KRI and data quality assessments per study CMP.
• Refresh the CM platform at defined frequency to enable signal identification.
• Create and maintain CM platform specifications and file in eTMF.
• Review study protocol and understand data sources, transfer specs and data structure.
• Peer-review CM platform setup performed by colleagues.

Skills

SAS programming

Data analysis

Communication

Organization

Autonomy

Tools

Cluepoints

Relational databases

EDC systems

SAS macro language

Job description

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role. The CMA will support centralized monitoring activities, set up QTLs/KRIs, and refresh CM platforms according to CMPs, while coordinating with clinical teams and stakeholders.

The role requires SAS programming expertise, knowledge of Cluepoints, and strong communication and organizational skills to ensure compliant, quality data-driven monitoring across studies.