Azafata De Degustación — Madrid

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madrid, comunidad de madrid, España Staff Global Group Jornada completa

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Clinical Monitoring Analyst (Cluepoints) - Remote London, United Kingdom
Presente su candidatura después de leer los siguientes requisitos de habilidades y cualificaciones para este puesto.
Full time
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).
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 CMP
Refresh the Centralized Monitoring Platform at predefined frequency to enable signal identification
Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF
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
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 biostatistics
~2-3 years SAS experience including macro language
~ Ability 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 levels
~ Ability to work with limited close supervision.
~ Prior experience in a Data Management related field is required
~ Experience with relational databases, preferably Clinical Data Management and EDC Systems
~ Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices. xkdbapo
~ 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.
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