Senior Cost Accounting Analyst

Copeland; Albacete; Remote; EUR 60,000 - 90,000; Full time

Job summary

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote position across multiple study sites in Europe and beyond. The role focuses on Centralized Monitoring setup, programming, and ongoing refreshes, delivering CM insights for sponsor projects.

You will work with SAS programming, including macro language, and collaborate with the Centralized Monitoring Lead to shape CM strategy and data visualisations.

Qualifications

• Minimum 3 years in pharma R&D or related field with centralized monitoring.
• Proficient in SAS programming including macro language.
• Experience with Cluepoints and data management a plus.

Responsibilities

• Set up and program QTL, KRI and data quality assessments per CMP.
• Refresh CM platform at defined frequencies to enable signal detection.
• Prepare and maintain CM platform specifications and file in eTMF.
• Collaborate with CM Lead and study stakeholders to interpret data and ensure protocol understanding.

Skills

SAS programming

Strong communication

Organisational skills

Autonomous working

Tools

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

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