Fisioterapeuta/Osteópata En Centro De Pilates (Madrid)

Profepilates,Sl; Madrid; Remote; EUR 60,000 - 80,000; Full time

Job summary

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) to join a sponsor‑dedicated project with remote work options. The role focuses on setting up and refreshing the Centralized Monitoring platform in line with CMPs and study needs.

You will work with SAS programming, Cluepoints, data management and EDC systems, supporting the CM Lead and engaging stakeholders across functions. Fluency in English is essential.

Qualifications

• At least 3 years relevant experience in pharmaceutical R&D or related field.
• 2-3 years SAS experience including macro language.
• Knowledge/experience with Cluepoints.
• Ability to work autonomously and engage stakeholders.
• Understanding of basic statistical concepts.
• Experience with data management and/or biostatistics.
• Excellent written and spoken English.

Responsibilities

• Supports the Centralized Monitoring Lead in CM strategy development.
• Setup/Program QTL, KRI and Data Quality Assessments according to CMP.
• Refresh the Centralized Monitoring Platform at predefined frequency.
• Generate and maintain the CM platform specifications document.
• Review protocol and data sources for the study.
• Execute and document peer-review of CM platform setup.

Skills

Strong communication

Organisational skills

Problem solving

Autonomous work style

Stakeholder engagement

Tools

SAS programming

Cluepoints

EDC Systems

Relational databases

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

**This role is not eligible for UK visa sponsorship**

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