Clinical Monitoring Analyst (CMA)

Job Title: Centralized Monitoring Analyst (CMA) at IQVIA This unique role within IQVIA is for a Lead Programmer on Cluepoints, called a Centralized Monitoring Analyst (CMA), requiring strong communication and organizational skills. Experience with SAS programming is necessary. The role can be based remotely in various European countries or South Africa. This position is part of a sponsor-dedicated project, working directly with the client to manage deliverables. Main Responsibilities: Support the Centralized Monitoring Lead (CML) in developing a fit-for-purpose CM strategy, including identifying relevant CM elements such as QTLs, KRIs, data visualizations, and Data Quality Assessments. Set up and program QTLs, KRIs, and Data Quality Assessments according to the study\’s Centralized Monitoring Plan (CMP). Refresh the Centralized Monitoring Platform regularly to enable signal detection. Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF. Review and understand study protocols thoroughly. Understand data sources, transfer specifications, and data structure for the study. Perform peer-reviews of CM platform setups conducted by colleagues. Experience and Skills: Minimum of 3 years relevant experience in pharmaceutical research, development, or related fields, preferably in centralized monitoring, data management, or biostatistics. 2-3 years of SAS experience, including macro language, is preferred. Ability to work autonomously and engage with stakeholders to execute centralized monitoring activities. Basic understanding of statistical analysis concepts and interpretation of outcomes. Ability to maintain data confidentiality. Self-motivated with minimal supervision. Strong communication, interpersonal, organizational, and problem-solving skills. High initiative, drive, and commitment. Prior experience in Data Management is required. Experience with relational databases, Clinical Data Management, and EDC Systems. Experience communicating across all organizational levels and working in collaborative teams globally. Knowledge of federal regulations, GCP, and Good Clinical Data Management Practices. Excellent command of English, both verbal and written. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. We aim to accelerate the development and commercialization of medical treatments to improve patient outcomes worldwide. Learn more at https://jobs.iqvia.com . We value diverse talent with curious minds and a commitment to innovation. Everyone at IQVIA contributes to our mission of improving lives globally. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled #J-18808-Ljbffr