Remote Power Platform & Rpa Innovator

Emais Servicios Integrales; Xanes; Remote; EUR 54,000 - 98,000; Full time

Job summary

IQVIA is seeking a Remote Clinical Monitoring Analyst with Cluepoints expertise to support the Centralized Monitoring Lead in executing CM strategies for sponsor projects. The role requires SAS programming skills, data interpretation, and collaboration with stakeholders across multiple sites.

The CMA will perform setup, programming and refreshes of the CM platform, ensuring CMP-aligned deliverables and maintenance of documentation in the eTMF system.

Qualifications

• Strong communication and organisation skills are required.
• Ability to work autonomously and coordinate with stakeholders.
• Experience in pharmaceutical research and development preferred.

Responsibilities

• Support Centralized Monitoring Lead in developing CM strategy.
• Set up/Program QTL, KRI and Data Quality Assessments per CMP.
• Refresh CM Platform to enable signal identification.
• Document CM platform specifications and file in eTMF.
• Understand study protocol and data sources for CM activities.
• Peer-review CM platform setup with CMA colleagues.

Skills

communication

organisation

autonomy

Tools

SAS

Macro language

Cluepoints

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