Operador De Almacén Remoto Y Preparación De Pedidos

Empresa De Gestión Y Selección; Segovia; Remote; EUR 81,000 - 107,000; Full time

Job summary

IQVIA is seeking a Clinical Monitoring Analyst (CMA) for Cluepoints to manage Centralized Monitoring activities remotely across multiple regions. The role requires collaboration with the Centralized Monitoring Lead and direct interaction with clients on delivery timelines.

The candidate should have 2-3 years SAS experience (including macro language) and knowledge of Cluepoints, with the ability to work autonomously and understand complex study data structures.

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
• Understanding of basic statistical analysis concepts and data confidentiality

Responsibilities

• Supports the Centralized Monitoring Lead in developing CM strategy and identifying CM elements for the study (QTL, KRI, data visualizations, Data Quality Assessments)
• Set up/program QTL, KRI and data quality assessments per study CMP
• Refresh CM platform at predefined frequency to enable signal identification
• Generate and maintain CM platform specifications document and file in eTMF
• Review and understand the study protocol
• Understand data sources, transfer specifications and data structure
• Execute and document peer-review of CM platform setup by colleagues

Skills

Autonomy

Stakeholder engagement

Communication skills

Statistical concepts

Tools

SAS

Job description

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