Recién Titulados/As Máster/ Grado Ingeniería Industrial/ Oficinas Centrales- Madrid . Programa [...]

Electren S.A.; Madrid; À distance; EUR 42 000 - 62 000; Plein temps

Résumé du poste

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role. You will support the Centralized Monitoring Lead by developing CM strategy elements and by programming QTLs, KRIs, and data quality assessments, across sponsor projects.

Responsibilities include refreshing the Centralized Monitoring Platform and delivering study CMP-aligned monitoring solutions; strong communication and organisational skills plus SAS programming experience are essential to ensure timely, high-quality

Qualifications

• Experience with SAS programming is necessary.

Responsabilités

• 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 CMP
• Refresh the Centralized Monitoring Platform

Connaissances

SAS programming

Description du poste

Clinical Monitoring Analyst (Cluepoints) - Remote

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Madrid, Spain
Full time
R
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 CMP
• Refresh the Centralized Monitoring Platform