Remote Centralized Monitoring Analyst (SAS/Cluepoints)

Tokio Marine HCC International; Barcelona; Remote; EUR 70,000 - 90,000; Full time

Job summary

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role. The position involves setting up and refreshing centralized monitoring platforms, developing CM strategies, and coordinating with stakeholders across multiple regions.

Strong SAS programming and English language proficiency are required. Responsibilities include CM platform programming, data quality assessments, and maintaining CM specifications while ensuring study CMP alignment.

Qualifications

• At least 3 years relevant experience in pharmaceutical research and development or related field, preferably 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 study CM processes
• Excellent English (verbal and written)

Responsibilities

• Supports Centralized Monitoring Lead in developing CM strategy and identifying CM elements for the study
• Set up and program QTL, KRI and Data Quality Assessments per study CMP
• Refresh Centralized Monitoring Platform at predefined frequencies
• Generate and maintain CM platform specifications document and file in eTMF
• Review and understand study protocol
• Understand data sources, transfer specs and data structure
• Perform peer-review of CM platform setup by colleagues

Skills

SAS programming

Communication skills

Organizational skills

Problem solving

Data confidentiality

Interpersonal skills

Tools

Cluepoints

Job description

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role. The position involves setting up and refreshing centralized monitoring platforms, developing CM strategies, and coordinating with stakeholders across multiple regions.

Strong SAS programming and English language proficiency are required. Responsibilities include CM platform programming, data quality assessments, and maintaining CM specifications while ensuring study CMP alignment.