Radiologist Full-time

Hace 1 semana

Sevilla, Metropolitana de Sevilla (comarca); Provincia de Sevilla; Andalucía, España Leader Clinics Jornada completa

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Clinical Monitoring Analyst (Cluepoints)
- Remote London, United KingdomBudapest, HungaryReading, Berkshire, United KingdomBloemfontein, South AfricaDublin, IrelandCenturion, South AfricaBarcelona, SpainSofia, BulgariaMadrid, SpainFull timeRThis 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 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 visualisations 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 centralised Monitoring, data management, and/or biostatistics2?3 years SAS experience 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 centralised monitoring processAbility to understand basic statistical analysis concepts and to interpret their outcomeAbility to maintain confidentiality of data and information during interactions with staff at all levelsAbility to work with limited close supervisionDemonstrated communication, interpersonal, organisational and problem-solving skillsHigh levels of initiative, drive and commitmentPrior 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 PracticesExcellent command, both verbal and written, of EnglishThis role is not eligible for UK visa sponsorshipEEO Minorities/Females/Protected Veterans/Disabled#J-*-Ljbffr

Radiologist Full-time

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