Enginyer/A D'Instal·Lacions: Líder De Projectes Pci (Remote 20%)

Cluster Enginyers; Barcelona; Remote; EUR 65,000 - 95,000; Full time

Job summary

IQVIA recruits a Clinical Monitoring Analyst (Cluepoints) for a sponsor-dedicated project, with remote work options. The role centers on setting up, programming, and refreshing the Centralized Monitoring platform using SAS and Cluepoints, aligned with the study CMP to ensure quality and timely deliveries.

You will interpret study protocols, manage data sources, and contribute to CM documentation while working autonomously and collaborating with global teams to protect data confidentiality and

Qualifications

• Minimum 3 years in pharma R&D or related field, centralized monitoring or data management.
• 2-3 years SAS experience including macro language.
• Experience with Cluepoints and knowledge of CM concepts.
• Ability to work autonomously and engage with stakeholders.
• Understanding of data sources, data transfer specs, and protocol basics.

Responsibilities

• Support CM Lead in developing CM strategy and study elements (QTL, KRI, data visuals).
• Setup/Program QTL, KRI, and data quality assessments per CMP.
• Refresh CM platform at defined frequency to enable signal detection.
• Produce and maintain CM platform specs and file in eTMF.
• Review study protocol and understand data structure.
• Peer-review CM platform setups performed by colleagues.

Skills

SAS programming

Communication

Organizational skills

Autonomy

Data management

Biostatistics

Cluepoints

Tools

SAS

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 levels
• Ability to work with limited close supervision.
• Demonstrated communication, interpersonal, organizational and problem-solving skills
• High levels of initiative, drive and commitment.
• Prior experience in a Data Management related field is required
• Experience with relational databases, preferably Clinical Data Management and EDC Systems
• Experience communicating with all levels of personnel and participating in collaborative work team (locally and globally).
• Advanced knowledge of federal regulations, Good Clinical Practice,