Remote CMA for Centralized Monitoring

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) to manage centralized monitoring activities remotely across multiple sites. You will set up QTL, KRI and Data Quality Assessments, refresh CM platforms, and ensure alignment with CMP while collaborating with global stakeholders.Candidates should have 3+ years in pharmaceutical R&D or related fields,...

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote, full-time role supported by a global study team. The CMA will program and refresh the Centralized Monitoring platform, aligning with the CMP and maintaining CM documentation in eTMF. Strong SAS programming, data management awareness, and excellent communication are essential. Candidate...

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) for a remote role across multiple locations. You will contribute to CM strategy, set up QTL/KRI, and refresh the CM platform while collaborating with the client to manage study deliveries.The role requires SAS programming experience, excellent English communication, and the ability to work autonomously...

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) to support centralized monitoring for sponsor-led projects. The role involves setup, programming, and refreshing the CM platform, with close collaboration with the Centralized Monitoring Lead and client teams. The candidate will work on CM elements such as QTL, KRIs, and data quality assessments, and...

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote, full-time role supported by a global study team. The CMA will program and refresh the Centralized Monitoring platform, aligning with the CMP and maintaining CM documentation in eTMF. Strong SAS programming, data management awareness, and excellent communication are essential. Candidate...

IQVIA is seeking a Clinical Monitoring Analyst (Remote) to lead the setup, programming and refresh of the Centralized Monitoring platform for sponsor projects. You will work with Cluepoints, perform QTL/KRI definitions, and ensure data quality assessments with strong communication to stakeholders. Requirements include 2–3 years SAS experience (including...

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote, sponsor-delivered project. The CMA will set up, program, and refresh the Centralized Monitoring platform in line with the study CMP, and will work with the Centralized Monitoring Lead and stakeholders to ensure timely signal detection. The role requires 2–3 years SAS experience...

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) for a sponsor-dedicated project. You will setup, program and refresh the Centralized Monitoring platform per the CMP, contributing to efficient signal detection and data quality across studies. A SAS programmer with 2–3 years plus data management/biostatistics experience is essential; strong...

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...