Senior Java Developer - Remote

Miratech; Málaga; A distancia; EUR 45.000 - 65.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a fully remote role. The CMA will work with sponsor clients to manage deliveries and oversee the Centralized Monitoring process, including setup, programming and refreshes of the CM platform according to CMP.

The role emphasizes strong communication and organisational skills, with SAS programming experience required to support QTLs, KRIs, data visualizations and Data Quality Assessments across studies.

Formación

• Requires experience with SAS programming.
• Role as Centralized Monitoring Analyst (CMA) with strong communication and organisation skills.

Responsabilidades

• Supports CM Lead in developing CM strategy elements (QTLs, KRIs, data visualizations, Data Quality Assessments).
• Setup/Program QTL, KRI and Data Quality Assessments per CMP.
• Refresh Centralized Monitoring Platform at predefined frequency to enable signal identification.
• Generate and maintain CM platform specifications document and file in eTMF.
• Review and understand study protocol.
• Understand data sources for the study.

Conocimientos

SAS programming

Centralized Monitoring

Descripción del empleo

Clinical Monitoring Analyst (Cluepoints) - Remote

London, United Kingdom
Budapest, Hungary
Reading, Berkshire, United Kingdom
Bloemfontein, South Africa
Dublin, Ireland
Centurion, South Africa
Barcelona, Spain
Sofia, Bulgaria
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

• 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 at predefined frequency to enable signal identification
• Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF
• Review and understanding of protocol is key
• Understand the data sources for the study, the data