Full-Time SR Clinical Data Systems Designer

• Lead or support the design and implementation of clinical databases in EDC systems.
• Manage and apply customer change requests to existing study builds.
• Troubleshoot EDC/system-related issues.
• Support system integrations, custom reporting, and advanced EDC module setups.
• Assist with analytical reporting configuration for study teams and sponsors.
• Collaborate with Configuration Specialists to align builds.
• Provide program-level support and represent the design team in client meetings.
• Participate in or lead data validation activities.
• Conduct hands-on clinical and external data review/reconciliation as needed.
• Contribute to internal guidance documentation and process improvement initiatives.
• Support development and review of departmental SOPs.
• Mentor, supervise, and train junior team members and peers as needed.

• Bachelor’s degree or higher in biomedical sciences, life sciences, or related discipline.
• Certification in Rave (Classic or RaveX), Veeva EDC, or other recognized EDC platforms is highly desirable.
• 2–4 years of experience in a technical designer or database architect role within clinical data systems.

• Strong understanding of clinical trial workflows and data standards.
• Proficient with Microsoft Office and one or more EDC platforms (Rave, RaveX, Veeva, etc.).

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