Remote Clinical Trial Monitoring Analyst with SAS

Melt Group; Valencia; Remote; EUR 65,000 - 90,000; Full time

Job summary

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) to join a sponsor-dedicated project, working remotely across multiple locations including Europe. The CMA will handle setup, programming and refresh of the Centralized Monitoring platform per CMP, requiring SAS programming experience.

Key duties include contributing to CM strategy, programming QTLs, KRIs and data quality assessments, maintaining CM platform specs, and collaborating with CM Lead and stakeholders to ensure study

Qualifications

• Minimum 3 years in pharmaceutical R&D or related field, centralized monitoring preferred.
• Experience with data management or biostatistics is a plus.
• Strong communication and organisational skills.

Responsibilities

• Support Centralized Monitoring Lead in CM strategy development and CM elements.
• Set up and program QTL, KRI and Data Quality Assessments per CMP.
• Refresh CM platform regularly to enable signal detection.
• Prepare CM platform specifications and file in eTMF.
• Understand study protocol and data sources; ensure data transfer specs.

Skills

SAS programming

Cluepoints knowledge

Communication skills

Tools

SAS macro language

Job description

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) to join a sponsor-dedicated project, working remotely across multiple locations including Europe. The CMA will handle setup, programming and refresh of the Centralized Monitoring platform per CMP, requiring SAS programming experience.

Key duties include contributing to CM strategy, programming QTLs, KRIs and data quality assessments, maintaining CM platform specs, and collaborating with CM Lead and stakeholders to ensure study