Remote Centralized Monitoring Analyst (CMA) – SAS Expert

Nascor-Formaci; Barcelona; Remote; EUR 62,000 - 98,000; Full time

Job summary

IQVIA is seeking a Clinical Monitoring Analyst (CMA) for Cluepoints to support centralized monitoring activities. You will set up and refresh the CM platform, perform data quality assessments, and coordinate with the Centralized Monitoring Lead and stakeholders across the study.

The role requires 3+ years in pharma R&D or related fields, SAS experience with macros, and strong English communication. This is a remote position with global collaboration and strict regulatory compliance.

Qualifications

• At least 3 years relevant experience in pharmaceutical R&D or related field, preferably centralized Monitoring, data management, or biostatistics.
• 2-3 years SAS experience including macro language.
• Knowledge/experience working on Cluepoints.
• Autonomous with ability to engage stakeholders to execute study-level CM processes.
• Understand basic statistical analysis concepts and interpret results.
• High initiative, drive and commitment.
• Experience in Data Management field is required.
• Experience with relational databases, CDM and EDC systems.
• Experience communicating with all levels in global teams.
• Advanced knowledge of federal regulations, GCP and CDMS practices.
• Excellent command of English (verbal and written).

Responsibilities

• Supports the Centralized Monitoring Lead in developing CM strategy and identifying CM elements for the study (QTL, KRI, data visualizations, data quality assessments).
• Setup/Program QTL, KRI and Data Quality Assessments per the CMP.
• Refresh the Centralized Monitoring Platform at predefined frequencies to enable signal detection.
• Generate and maintain CM platform specifications and file in eTMF.
• Review and understand the study protocol.
• Understand data sources, data transfer specs, and data structure.
• Perform peer-review of CM platform setups.

Skills

SAS programming

Data management

CDM experience

Regulatory knowledge

English proficiency

Job description

IQVIA is seeking a Clinical Monitoring Analyst (CMA) for Cluepoints to support centralized monitoring activities. You will set up and refresh the CM platform, perform data quality assessments, and coordinate with the Centralized Monitoring Lead and stakeholders across the study.

The role requires 3+ years in pharma R&D or related fields, SAS experience with macros, and strong English communication. This is a remote position with global collaboration and strict regulatory compliance.