Remote Clinical Monitoring Analyst (Cluepoints)

Unode50

Barcelona

Remote

EUR 60.000 - 90.000

Vollzeit

Vor 2 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Benefits dieser Stelle

Remote work

Zusammenfassung

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote, sponsor-driven project. The CMA will set up, program, and refresh the Centralized Monitoring platform per CMP, with strong SAS programming and data management requirements.

You will work with the Centralized Monitoring Lead and clients to deliver CM outcomes across multiple regions. You will contribute to CM strategy development, ensure data sources and protocols are understood, and maintain documentation in the eTMF

Qualifikationen

  • Experience in pharmaceutical research or centralized monitoring is required.
  • 2-3 years SAS experience including macro language.
  • Knowledge/ experience working on Cluepoints is preferred.
  • Excellent communication and organisational skills.

Aufgaben

  • Supports the Centralized Monitoring Lead in developing CM strategy and QTL/KRI data visualizations.
  • Setup/program QTL, KRI, and Data Quality Assessments per CMP.
  • Refresh CM platform at predefined frequency to enable signal identification.
  • Generate CM platform specifications and maintain documentation in eTMF.
  • Review study protocol and understand data sources and transfer specs.
  • Perform peer-review of CM platform setup and collaborate with CM teams.

Jobbeschreibung

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote, sponsor-driven project. The CMA will set up, program, and refresh the Centralized Monitoring platform per CMP, with strong SAS programming and data management requirements.

You will work with the Centralized Monitoring Lead and clients to deliver CM outcomes across multiple regions. You will contribute to CM strategy development, ensure data sources and protocols are understood, and maintain documentation in the eTMF

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