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Role Overview:

  • Support clinical research operations through reliable CTMS configuration and quality control.
  • Collaborate with study teams to translate platform data into actionable insights.
  • Contribute to platform governance, incident management, and process improvement.

Key Responsibilities:

  • Configure CTMS study and site builds, including visits, procedures, schedules, and financial elements.
  • Execute quality-control checklists, validate configurations, and escalate defects as needed.
  • Provide technical CTMS support, manage access requests, and deliver user training.

Requirements:

  • 2–4 years of experience in CTMS, clinical platforms, or clinical systems.
  • Working knowledge of CTMS configuration and study-build processes.
  • Proficiency with data analysis, reporting, and documentation.

Benefits:

  • Medical, dental, and vision insurance plan options.
  • Predominantly remote work from Brazil with flexible in-person activities.
  • Opportunities to develop technical and clinical operations expertise.

Partner Company

This company supports clinical research operations through reliable CTMS configuration and quality control. It fosters a collaborative, remote-friendly environment where detail-oriented analysts contribute to efficient clinical delivery.

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