Intern SR Clinical Data Systems Designer

• Lead or support the design and implementation of clinical databases in EDC systems, including programming data validation checks (automated/manual).
• Manage and apply customer change requests to existing study builds.
• Troubleshoot EDC/system-related issues and contribute to continuous improvement initiatives.
• Support or lead 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 with company and sponsor standards.
• Provide program-level support and represent the design team in client meetings.
• Participate in or lead data validation activities before and after go-live.
• 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 — or equivalent relevant experience.
• 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.).
• Familiarity with programming or scripting languages such as SQL, VBA, or C# is a plus.

• Proficiency in English (spoken and written).
• Strong problem-solving and analytical thinking.
• Excellent communication and team collaboration.

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