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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.