Join Bioforum - Where Innovation Meets Opportunity! We’re on the lookout for a Senior Clinical Data Systems Designer (Technical Designer / Database Architect) to join our dynamic, growing team. If you're certified in Medidata Rave, RaveX, Veeva EDC, or any other industry-recognized EDC platform and you’re ready to take the next technical step in your career, we want to hear from you! Why Bioforum? We are a vibrant, quality-driven company that values innovation, collaboration, and the professional growth of our team. Be part of building smarter systems for better clinical data. Minimum Qualifications: 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. Minimum Experience: 2–4 years of experience in a technical designer or database architect role within clinical data systems. Key Skills: 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. Core Competencies: Proficiency in English (spoken and written). Strong problem-solving and analytical thinking. Excellent communication and team collaboration. Key Responsibilities: 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. Apply Now!Ready to design the future of clinical trials? Send your CV to the Bioforum team today. We're always looking for talented, quality-driven individuals to join our journey. #J-18808-Ljbffr