Remote Centralized Monitoring Analyst (Cluepoints)

Leader Clinics

Pena Laza

Remote

EUR 60,000 - 90,000

Full time

5 days ago
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Job summary

IQVIA is seeking a Remote Clinical Monitoring Analyst (CMA) for Cluepoints. The role requires SAS programming skills and experience with centralized monitoring in pharma R&D.

You will collaborate with the CM Lead and sponsor teams to implement study CMPs, QTLs and data quality assessments across multiple geographies. Responsibilities include setting up CM elements, refreshing the CM platform, documenting specifications, and ensuring data protocol alignment.

Qualifications

  • 3+ years in pharma R&D or centralised monitoring, data management or biostatistics.
  • 2–3 years SAS experience including macro language.
  • Knowledge/experience with Cluepoints platform.
  • Autonomous work style with stakeholders.
  • Understanding of basic statistical concepts.
  • Confidentiality of data handling.
  • Ability to work with limited supervision.
  • Strong communication, interpersonal and organisational skills.
  • High initiative and drive.
  • Experience in Data Management is preferred.
  • Experience with relational databases and EDC systems.
  • Proficiency in English (oral and written).

Responsibilities

  • Support CM Lead in developing CM strategy and identify CM elements for the study (QTL, KRI, data visualisations, DQA).
  • Setup/program QTL, KRI and DQA per study CMP.
  • Refresh CM platform at defined frequency for signal identification.
  • Create/maintain CM platform specifications document and store in eTMF.
  • Understand protocol and study data sources, transfer specs and data structure.
  • Peer-review CM platform setup performed by CMA colleagues.

Skills

SAS programming
Cluepoints
Data management
Communication
Problem solving

Tools

Relational databases
EDC systems

Job description

IQVIA is seeking a Remote Clinical Monitoring Analyst (CMA) for Cluepoints. The role requires SAS programming skills and experience with centralized monitoring in pharma R&D.

You will collaborate with the CM Lead and sponsor teams to implement study CMPs, QTLs and data quality assessments across multiple geographies. Responsibilities include setting up CM elements, refreshing the CM platform, documenting specifications, and ensuring data protocol alignment.

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