Remote Centralized Monitoring Analyst (SAS, Cluepoints)

Extia Group; Barcelona; Remote; EUR 60,000 - 90,000; Full time

Job summary

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) to join a sponsor-dedicated project remotely. You will setup, program and refresh the Centralized Monitoring platform, aligning with the CMP and QA requirements. Strong SAS scripting and data management expertise are essential.

You will collaborate closely with the Centralized Monitoring Lead and client teams to ensure CM deliverables, data integrity and regulatory compliance across multiple study sites.

Qualifications

• 3+ years of experience in pharmaceutical R&D or related field, preferably centralized monitoring, data management, or biostatistics
• 2-3 years SAS experience including macro language
• Experience with Cluepoints
• Ability to work autonomously and coordinate with stakeholders
• Strong communication, interpersonal, organizational and problem-solving skills
• High initiative and commitment
• Experience with data management and relational databases (CDM/EDC)
• Experience communicating with all levels of staff and cross-functional teams
• Familiarity with GCP/ICH regulatory requirements and GxP
• Excellent written and verbal English skills

Responsibilities

• Set up, program and refresh the Centralized Monitoring platform per CMP
• Assist in developing CM strategy and identify CM elements (QTL, KRI, data visualizations)
• Configure QTL, KRI and DQA per CMP and generate CM platform specs document
• Review study protocols and understand data sources, transfer specs and data structure
• Collaborate with CMA colleagues and perform peer-review of CM platform setup

Job description

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) to join a sponsor-dedicated project remotely. You will setup, program and refresh the Centralized Monitoring platform, aligning with the CMP and QA requirements. Strong SAS scripting and data management expertise are essential.

You will collaborate closely with the Centralized Monitoring Lead and client teams to ensure CM deliverables, data integrity and regulatory compliance across multiple study sites.