Remote Centralized Monitoring Analyst (Cluepoints)

Irium; Madrid; Remote; EUR 65,000 - 90,000; Full time

Job summary

IQVIA invites a Clinical Monitoring Analyst (Cluepoints) to join a sponsor-driven project. This remote, full-time role requires strong SAS programming and the ability to manage CM deliverables directly with clients.

You will implement the Centralized Monitoring process by setting up QTLs, KRIs and data quality assessments, refreshing the CM platform regularly, and documenting specifications for eTMF. Collaborate with the Centralized Monitoring Lead and CMA colleagues across global sites to

Qualifications

• Minimum 3 years in pharma R&D or related field with centralized monitoring.
• 2-3 years SAS experience including macro language.
• Familiarity with Cluepoints platform is preferred.
• Ability to work autonomously and coordinate with study stakeholders.
• Understanding of data management concepts and data transfer specs.
• Excellent written and verbal English.

Responsibilities

• Support Centralized Monitoring Lead in developing CM strategy for the study.
• Set up and program QTLs, KRIs and Data Quality Assessments per CMP.
• Refresh the CM platform at defined frequencies to enable signal detection.
• Create and maintain CM platform specifications documents and file in eTMF.
• Review study protocol and data sources to ensure CM alignment.
• Collaborate with CMA colleagues across locations and communicate findings.

Skills

SAS programming

communication skills

organization skills

data management

biostatistics knowledge

English proficiency

Tools

Cluepoints

SAS

Job description

IQVIA invites a Clinical Monitoring Analyst (Cluepoints) to join a sponsor-driven project. This remote, full-time role requires strong SAS programming and the ability to manage CM deliverables directly with clients.

You will implement the Centralized Monitoring process by setting up QTLs, KRIs and data quality assessments, refreshing the CM platform regularly, and documenting specifications for eTMF. Collaborate with the Centralized Monitoring Lead and CMA colleagues across global sites to