Centralized Monitoring Lead - SAS & Cluepoints (Remote)

Scopely

Barcelona

Remote

EUR 55,000 - 75,000

Full time

4 days ago
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Job summary

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role, to support centralized monitoring activities across a sponsor project. Lead the setup, programming and refresh of the CM platform with strong SAS skills and clear stakeholder communication.

Key responsibilities include CM strategy development, QTL/KRI/DQA implementation, and maintaining CM specifications. Excellent English communication and a solid data-management background are required.

Qualifications

  • At least 3 years in pharmaceutical R&D or related field, preferably centralized monitoring, data management 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.
  • Excellent command of English (verbal and written).
  • Experience with relational databases, preferably CDM and EDC systems.
  • Familiarity with federal regulations, Good Clinical Practice, and GCDMP.

Responsibilities

  • Supports the Centralized Monitoring Lead in developing CM strategy by identifying relevant CM elements for the study (QTL, KRI, data visualizations, DQA).
  • Set up/program QTL, KRI and Data Quality Assessments per CMP.
  • Refresh the Centralized Monitoring Platform at defined frequency to enable signal identification.
  • Generate and maintain CM platform specifications document and file in eTMF.
  • Review and understanding of study protocol.
  • Understand data sources, transfer specs and data structure.
  • Execute and document peer-review of CM platform setup by CMA colleagues.

Skills

SAS programming
Cluepoints knowledge
communication
organization
statistical concepts
data management
biostatistics
confidentiality
team collaboration

Tools

Cluepoints

Job description

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role, to support centralized monitoring activities across a sponsor project. Lead the setup, programming and refresh of the CM platform with strong SAS skills and clear stakeholder communication.

Key responsibilities include CM strategy development, QTL/KRI/DQA implementation, and maintaining CM specifications. Excellent English communication and a solid data-management background are required.

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