Junior Treasury Operations Analyst - Reconciliations & Fx

Remoteo; Málaga; À distance; EUR 58 000 - 85 000; Plein temps

Résumé du poste

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) to join a sponsor-dedicated project and manage CM deliveries remotely. The role centers on setup, programming, and refreshing the Centralized Monitoring platform according to the CMP, with collaboration across global teams and strong SAS proficiency.

The ideal candidate will have 3+ years in pharma R&D or related fields, experience with Cluepoints, data management, and the ability to work autonomously while communicating effectively

Qualifications

• At least 3 years in pharmaceutical R&D or related field, preferably centralized Monitoring, data management, and/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 activities.

Responsabilités

• Support CM strategy development by contributing to CM elements (QTL, KRIs, data visuals, DQA).
• Set up/program QTL, KRI, and DQA per the CMP.
• Refresh the CM platform at defined cadence to identify signals.
• Generate and maintain CM platform specifications and file in eTMF.
• Review study protocol to ensure CM alignment.
• Understand data sources, transfer specs, and data structure.
• Peer-review CM platform setup performed by colleagues.

Connaissances

communication skills

organizational skills

autonomy

problem-solving

interpersonal skills

Outils

SAS programming

Cluepoints

EDC systems

relational databases

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).

• 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, and Good Clinical Data Management Practices.
• Excellent command, both verbal and