Lead Centralized Monitoring Analyst (SAS)

Iqvia; Barcelona; A distancia; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

IQVIA in Barcelona seeks a Lead Programmer (Centralized Monitoring Analyst) with strong SAS programming and excellent communication. This role supports sponsor projects, managing CM platform setup and refreshes per CMP, and ensuring data quality through QTL and KRIs.

The position requires 3+ years in pharma data management or related fields, SAS with macros, Cluepoints experience, and autonomy to collaborate with global teams. Not eligible for UK visa sponsorship.

Formación

• At least 3 years relevant experience in pharmaceutical R&D 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 and engage with stakeholders to execute study-level CM processes.
• Ability to understand basic statistical concepts and interpret outcomes.
• Excellent command, both verbal and written, of English.

Responsabilidades

• Supports the Centralized Monitoring Lead (CML) in developing a fit-for-purpose CM strategy by identifying CM elements for the study (QTL, KRIs, data visualizations, and Data Quality Assessments).
• Setup/Program QTL, KRI and Data Quality Assessments per the study CMP.
• Refresh the Centralized Monitoring Platform at predefined frequency to enable signal identification.
• Generate and maintain CM platform specifications document and file in eTMF.
• Review and understanding of protocol is key.
• Understand data sources, data transfer specs and data structure.
• Execute and document peer-review of CM platform setup done by others.

Conocimientos

Communication skills

Organisation skills

Autonomy

Problem solving

Interpersonal skills

English proficiency

Herramientas

SAS

Cluepoints

Relational databases

EDC systems

Descripción del empleo

IQVIA in Barcelona seeks a Lead Programmer (Centralized Monitoring Analyst) with strong SAS programming and excellent communication. This role supports sponsor projects, managing CM platform setup and refreshes per CMP, and ensuring data quality through QTL and KRIs.

The position requires 3+ years in pharma data management or related fields, SAS with macros, Cluepoints experience, and autonomy to collaborate with global teams. Not eligible for UK visa sponsorship.