Remote Cluepoints Clinical Monitoring Analyst (SAS)

Seleccion E Formacion

Valencia

Remote

EUR 80,000 - 107,000

Full time

3 days ago
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Job summary

IQVIA invites applications for a Remote Clinical Monitoring Analyst (Cluepoints). The role supports the Centralized Monitoring Lead in developing CM strategies and executing CM processes for sponsor-driven studies.

You will setup, program, and refresh the CM platform, review study protocols, and manage data sources and documentation with a focus on data quality and regulatory compliance. You will collaborate with global teams, demonstrate strong communication and organizational skills, and work

Qualifications

  • 3+ years in pharmaceutical R&D or related field, preferably in centralized monitoring, data management or biostatistics.
  • SAS experience including macro language (2-3 years).
  • Experience with Cluepoints preferred.
  • Ability to work autonomously and liaise with stakeholders to execute CM activities.
  • Strong communication and problem-solving skills, with initiative.

Responsibilities

  • Perform setup, programming and refreshes of the Centralized Monitoring platform according to CMP.
  • Develop CM strategy components (QTL, KRI, data visualizations, data quality assessments).
  • Setup/Program QTL, KRI and DQA per CMP.
  • Refresh CM platform at predefined frequency to enable signal ID.
  • Document CM platform specifications and file in eTMF.
  • Understand study protocol and data sources.

Skills

SAS programming
Centralized Monitoring
Data management
Biostatistics
Communication skills
Regulatory knowledge
English proficiency

Tools

Cluepoints
SAS Macro language
Relational databases

Job description

IQVIA invites applications for a Remote Clinical Monitoring Analyst (Cluepoints). The role supports the Centralized Monitoring Lead in developing CM strategies and executing CM processes for sponsor-driven studies.

You will setup, program, and refresh the CM platform, review study protocols, and manage data sources and documentation with a focus on data quality and regulatory compliance. You will collaborate with global teams, demonstrate strong communication and organizational skills, and work

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