This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary. This role is part of a sponsor dedicated project where you will be working with the client directly to manage deliveries.The CMA contributes to the execution of the Centralized Monitoring process by performing the setup, programming and refresh(es) of the Centralized Monitoring platform, according to the study-specific Centralized Monitoring Plan (CMP).Main responsibilities include:Supports the Centralized Monitoring Lead (CML) in the development of the fit-for purpose CM strategy by contributing to the identification of the relevant CM elements to be implemented for the study (Quality Tolerance Limits (QTL), Key Risk Indicators, data visualizations and Data Quality Assessments)Setup/Program QTL, KRI and Data Quality Assessments according to the study CMPRefresh the Centralized Monitoring Platform at predefined frequency to enable signal identificationGenerate and maintain the Centralized Monitoring Platform specifications document and file it in eTMFReview and understanding of protocol is keyUnderstand the data sources for the study, the data transfer specifications and the data structureExecute and document peer-review of CM platform setup done by other CMA colleaguesExperience:At least 3 years relevant experience in the area of pharmaceutical research and development or related field preferably in centralized Monitoring, data management, and/or biostatistics2-3 years SAS experience preferred including macro languageKnowledge/ experience working on CluepointsAbility to work in an autonomous way and engage with relevant stakeholders to execute activities related to study level centralized monitoring process.Ability to understand basic statistical analysis concepts and to interpret their outcome.Ability to maintain confidentiality of data and information during interactions with staff at all levelsAbility to work with limited close supervision.Demonstrated communication, interpersonal, organizational and problem-solving skillsHigh levels of initiative, drive and commitment.Prior experience in a Data Management related field is requiredExperience with relational databases, preferably Clinical Data Management and EDC SystemsExperience communicating with all levels of personnel and participating in collaborative work team (locally and globally).Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices.Excellent command, both verbal and written, of EnglishThis role is not eligible for UK visa sponsorshipIQVIA 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 commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more