Remote Centralized Monitoring Analyst (SAS)

Encompass Care Clinical Counseling

Salamanca

Remote

EUR 80,000 - 116,000

Full time

6 days ago
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Job summary

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) for a remote, full-time role. You will support the centralized monitoring program, set up QTLs and KRIs, and refresh CMP-driven CM platforms, coordinating with the CM Lead and stakeholders.

The role requires SAS programming experience (including macros), strong communication, and the ability to interpret data within GMP/compliance frameworks. Collaboration across global teams is essential.

Qualifications

  • 3+ years in pharmaceutical research and development or related field focusing on centralized monitoring, data management, or biostatistics.
  • SAS experience including macro language is required.
  • Experience working with Cluepoints is preferred.
  • Ability to work autonomously and coordinate with stakeholders to execute CM activities.
  • Strong understanding of statistical concepts and data confidentiality.

Responsibilities

  • Support CM Lead in developing CM strategy by identifying CM elements to implement for the study.
  • Set up and program QTLs, KRIs, and Data Quality Assessments per CMP.
  • Refresh CM platform at defined cadence for signal detection.
  • Prepare CM platform specifications document and file in eTMF.
  • Interpret study protocol and data transfer specs to inform CM setup.
  • Collaborate with CMA colleagues for peer-review of CM platform setups.

Skills

SAS programming
Strong communication
Organizational skills
Autonomous working
Data interpretation
Problem solving
SAS macro language

Tools

SAS
Cluepoints

Job description

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) for a remote, full-time role. You will support the centralized monitoring program, set up QTLs and KRIs, and refresh CMP-driven CM platforms, coordinating with the CM Lead and stakeholders.

The role requires SAS programming experience (including macros), strong communication, and the ability to interpret data within GMP/compliance frameworks. Collaboration across global teams is essential.

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