Remote Centralized Monitoring Analyst — SAS & Cluepoints

Euraxess

Barcelona

Remote

EUR 55,000 - 90,000

Full time

3 days ago
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Job summary

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role across Europe to manage the setup, programming and refreshes of the Centralized Monitoring platform in line with the CMP. You will work with the client directly to deliver CM outcomes and ensure data confidentiality and regulatory compliance.

Ideal candidates have 3+ years in pharma R&D or related fields, 2-3 years SAS experience (including macros), and strong communication skills to collaborate with cross-functional

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 on study-level CM processes.
  • Excellent written and verbal communication, organisational and problem-solving skills.
  • Advanced knowledge of federal regulations, GCP and CDMP will help.

Responsibilities

  • Set up and program the Centralized Monitoring platform per CMP.
  • Refresh the Centralized Monitoring Platform at predefined frequency to identify signals.
  • Generate and maintain CM platform specifications and file in eTMF.
  • Review protocol and understand data sources, transfer specs and data structure.
  • Execute peer-review of CM platform setup by colleagues.

Skills

SAS programming
Data management
Biostatistics
Communication
Problem solving

Tools

Cluepoints
Relational databases
EDC Systems

Job description

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role across Europe to manage the setup, programming and refreshes of the Centralized Monitoring platform in line with the CMP. You will work with the client directly to deliver CM outcomes and ensure data confidentiality and regulatory compliance.

Ideal candidates have 3+ years in pharma R&D or related fields, 2-3 years SAS experience (including macros), and strong communication skills to collaborate with cross-functional

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