Profesor/A De Matemáticas Remoto Para Secundaria

Globeducate; Granada; Remote; EUR 70,000 - 90,000; Full time

Job summary

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) for a remote, full-time role. You will work on centralized monitoring activities, setting up QTLs, KRIs, and data quality assessments, and refreshing the CM platform to detect signals. Strong SAS programming skills and experience with Cluepoints are required.

You will collaborate with a sponsor-driven project team to ensure CMP adherence and documentation in eTMF, with autonomy and clear communication essential for success.

Qualifications

• At least 2–3 years SAS experience including macro language.
• Experience with pharmacovigilance or centralized monitoring is preferred.
• Ability to work autonomously and engage with stakeholders to deliver CMP activities.
• Ability to understand basic statistical concepts and interpret results.

Responsibilities

• Set up and program QTL, KRI and Data Quality Assessments per the CMP.
• Refresh the CM platform at defined frequencies to enable signal detection.
• Prepare and maintain CM platform specifications and documentation in eTMF.
• Collaborate with CM Lead and other CMA colleagues to ensure protocol understanding.

Skills

SAS programming

Data analysis concepts

Communication & organisation

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
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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