Administrativo De Fincas: Gestión De Comunidades En Madrid

Housfy Real Estate, S.L.; Madrid; Remote; EUR 60,000 - 85,000; Full time

Job summary

Cluepoints, a remote role in Europe, seeks a Clinical Monitoring Analyst to support the CM Lead by creating and maintaining the centralized monitoring platform and CM strategy. You will program QTL, KRIs and data quality assessments and ensure alignment with the study CMP.

The role requires strong SAS skills, experience with Cluepoints, and the ability to work independently with global stakeholders to drive data-driven monitoring decisions.

Qualifications

• 3+ years in pharmaceutical research and development, centralized monitoring, data management, or biostatistics.
• 2+ years SAS experience including macro language.
• Experience with Cluepoints platform.
• Ability to work autonomously and engage with stakeholders to execute study-level CM processes.
• Good understanding of data sources, data transfer specs and data structures.

Responsibilities

• Supports the Centralized Monitoring Lead in developing CM strategy and implementing CM elements (QTL, KRI, data visualisations).
• Set up and program QTL, KRI, and Data Quality Assessments per the CMP.
• Refresh Centralized Monitoring Platform at defined frequency for signal detection.
• Create and maintain CM platform specifications documents and file in eTMF.
• Understand study protocol and data sources to ensure accurate CM processes.
• Peer-review CM platform setup performed by colleagues.

Skills

SAS

Data management

Biostatistics

Communication

Team collaboration

GCP/QA familiarity

Tools

Cluepoints

EDC Systems

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

Main responsibilities

• 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 visualisations 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, organisational 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**

EEO Minorities/Females/Protected Veterans/Disabled