Auxiliar De Cocina Y Limpieza - Madrid Centro

Glh Singular Restaurants; Madrid; À distance; EUR 60 000 - 90 000; Plein temps

Résumé du poste

IQVIA is seeking a Clinical Monitoring Analyst (CMA) for the Cluepoints platform. The role is remote with multiple country options and requires strong SAS programming skills and experience in centralized monitoring.

You will support the Centralized Monitoring Lead, set up QTLs, KRIs and data quality assessments, refresh CM platform per CMP, and collaborate with stakeholders to ensure study deliveries.

Qualifications

• At least 3 years in pharmaceutical R&D or related field with centralized monitoring, data management or biostatistics.
• 2–3 years SAS experience including macro language.
• Knowledge/experience working on Cluepoints.
• Ability to work autonomously and engage with stakeholders to execute CM activities.
• Ability to understand protocol and data sources for the study.

Responsabilités

• Supports the Centralized Monitoring Lead in developing the Centralized Monitoring strategy and CM elements for the study.
• Setup/Program QTL, KRI and Data Quality Assessments according to the CMP.
• Refresh the Centralized Monitoring Platform at predefined frequency to enable signal identification.
• Generate and maintain the Centralized Monitoring Platform specifications document in eTMF.
• Review and understanding of protocol; identify data sources and data transfer specs.
• Perform peer-review of CM platform setup and document findings.

Connaissances

SAS programming

Macro language

Centralized Monitoring

Data management

Communication skills

Autonomous working

Outils

Cluepoints

Description du poste

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 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 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 transfer specifications and the data structure
+ Execute and document peer-review of CM platform setup done by other CMA colleagues
Experience:
+ 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
+ Knowledge/ experience working on Cluepoints
+ 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.
+ Demonstrated communication, interpersonal