Remote Centralized Monitoring Analyst (SAS) – Cluepoints

Sumar; Gerona; Remote; EUR 70,000 - 99,000; Full time

Job summary

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) to lead centralized monitoring activities on sponsor projects in a remote capacity. Strong SAS programming and data management skills are required to program CM elements and support data quality assessments.

The CMA will set up, refresh, and maintain the CM platform per CMP, collaborate with the Centralized Monitoring Lead, and ensure regulatory compliance while communicating with global stakeholders. English proficiency is essential.

Qualifications

• At least 3 years of experience in pharmaceutical R&D or related field, preferably centralized Monitoring, data management, or biostatistics.
• Experience with SAS including macro language.
• Knowledge/experience with Cluepoints.
• Ability to work autonomously and coordinate with stakeholders to execute CM activities.
• Understanding of basic statistical concepts and data interpretation.
• Ability to maintain data confidentiality and work with limited supervision.
• Excellent written and verbal communication, organizational and problem-solving skills.
• Experience with relational databases and Clinical Data Management and EDC systems.

Responsibilities

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

Skills

SAS programming

Data management

Biostatistics

Communication

Problem-solving

GxP knowledge

Tools

Cluepoints

SAS

Job description

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) to lead centralized monitoring activities on sponsor projects in a remote capacity. Strong SAS programming and data management skills are required to program CM elements and support data quality assessments.

The CMA will set up, refresh, and maintain the CM platform per CMP, collaborate with the Centralized Monitoring Lead, and ensure regulatory compliance while communicating with global stakeholders. English proficiency is essential.