Lead Clinical Monitoring Analyst - Remote

Staff Global Group; Madrid; Remoto; EUR 60.000 - 95.000; Tempo pieno

Descrizione del lavoro

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) to work remotely on sponsor-led projects. You will support the Centralized Monitoring Lead, set up and program QTLs, KRIs and data quality assessments using SAS, and coordinate with global stakeholders.

The role requires 3+ years in pharma R&D or related fields, including experience with Cluepoints, data management and EDC systems, with excellent English and autonomous working style.

Competenze

• 3+ years in pharma R&D or 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 to execute CM activities.
• Strong communication, interpersonal, organisational and problem-solving skills.
• Experience with relational databases, Clinical Data Management and EDC systems.
• Excellent command, both verbal and written, of English.

Mansioni

• Supports the Centralized Monitoring Lead in developing the fit-for-purpose CM strategy by contributing to relevant CM elements.
• Setup/Program QTL, KRI and Data Quality Assessments according to the CMP.
• Refresh the Centralized Monitoring Platform at predefined frequency to enable signal identification.
• Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF.
• Review and understanding of protocol is key.
• Understand the data sources for the study, the data transfer specifications and the data structure.
• Execute and document peer-review of CM platform setup done by other CMA colleagues.

Conoscenze

SAS programming

Cluepoints

Centralized Monitoring

Strumenti

EDC Systems

eTMF

Descrizione del lavoro

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) to work remotely on sponsor-led projects. You will support the Centralized Monitoring Lead, set up and program QTLs, KRIs and data quality assessments using SAS, and coordinate with global stakeholders.

The role requires 3+ years in pharma R&D or related fields, including experience with Cluepoints, data management and EDC systems, with excellent English and autonomous working style.