Clinical Monitoring Analyst

3 weeks ago


WorkFromHome, South Africa IQVIA Full time

Clinical Monitoring Analyst (Cluepoints) - Remote Join to apply for the Clinical Monitoring Analyst (Cluepoints) - Remote role at IQVIA . This unique role within IQVIA is for a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisational skills. Experience with SAS programming is necessary. The CMA is part of a sponsor dedicated project and will work directly with the client to manage deliveries. Responsibilities Supports the Centralized Monitoring Lead (CML) in developing a fit-for-purpose CM strategy, contributing to the identification of the relevant CM elements to be implemented for the study (QTL, KRI, data visualisations and Data Quality Assessments). Setup/Program QTL, KRI and Data Quality Assessments according to the study CMP. Refresh the Centralized Monitoring Platform at a predefined frequency to enable signal identification. Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF. Review and understand the protocol. Understand the data sources for the study, the data transfer specifications and the data structure. Execute and document peer‑review of CM platform setup done by other CMA colleagues. Experience and Qualifications At least 3 years of relevant experience in pharmaceutical research and development or a related field, preferably in centralised monitoring, data management, or biostatistics. 2‑3 years of SAS experience including macro language. Knowledge/experience working on Cluepoints. Ability to work autonomously and engage with stakeholders to execute activities related to study‑level centralised monitoring. Ability to understand basic statistical analysis concepts and interpret their outcomes. Ability to maintain confidentiality of data and information during interactions with staff at all levels. Ability to work with limited close supervision. Demonstrated communication, interpersonal, organisational and problem‑solving skills. High levels of initiative, drive and commitment. Prior experience in a Data Management field is required. Experience with relational databases, preferably Clinical Data Management and EDC Systems. Experience communicating with all levels of personnel and participating in collaborative teamwork (locally and globally). Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices. Excellent command, both verbal and written, of English. This role is not eligible for UK visa sponsorship. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialisation of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at #J-18808-Ljbffr



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