Senior Clinical Data System Designer

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    "description": "<p>Join Bioforum - Where Innovation Meets Opportunity!</p>\n<p><br>We’re on the lookout for a <span style=\"font-weight: bold;\">Senior Clinical Data Systems Designer</span> (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!</p>\n<p> </p>\n<p><span style=\"text-decoration: underline;\">Why Bioforum?</span><br>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.</p>\n<p> </p>\n<p><span style=\"font-weight: bold;\">Minimum Qualifications:</span></p>\n<ul>\n<li><span>Bachelor’s degree or higher in biomedical sciences, life sciences, or related discipline — or equivalent relevant experience.</span></li>\n<li><span>Certification in Rave (Classic or RaveX), Veeva EDC, or other recognized EDC platforms is highly desirable.</span></li>\n</ul>\n<p> </p>\n<p><span style=\"font-weight: bold;\">Minimum Experience:</span></p>\n<ul>\n<li><span>2–4 years of experience in a technical designer or database architect role within clinical data systems.</span></li>\n</ul>\n<p> </p>\n<p><span style=\"font-weight: bold;\">Key Skills:</span></p>\n<ul>\n<li><span>Strong understanding of clinical trial workflows and data standards.</span></li>\n<li><span>Proficient with Microsoft Office and one or more EDC platforms (Rave, RaveX, Veeva, etc.).</span></li>\n<li><span>Familiarity with programming or scripting languages such as SQL, VBA, or C# is a plus.</span></li>\n</ul>\n<p> </p>\n<p><span style=\"font-weight: bold;\">Core Competencies:</span></p>\n<ul>\n<li><span>Proficiency in English (spoken and written).</span></li>\n<li><span>Strong problem-solving and analytical thinking.</span></li>\n<li><span>Excellent communication and team collaboration.</span></li>\n</ul>\n<p> </p>\n<p><span style=\"font-weight: bold;\">Key Responsibilities:</span></p>\n<ul>\n<li><span>Lead or support the design and implementation of clinical databases in EDC systems, including programming data validation checks (automated/manual).</span></li>\n<li><span>Manage and apply customer change requests to existing study builds.</span></li>\n<li><span>Troubleshoot EDC/system-related issues and contribute to continuous improvement initiatives.</span></li>\n<li><span>Support or lead system integrations, custom reporting, and advanced EDC module setups.</span></li>\n<li><span>Assist with analytical reporting configuration for study teams and sponsors.</span></li>\n<li><span>Collaborate with Configuration Specialists to align builds with company and sponsor standards.</span></li>\n<li><span>Provide program-level support and represent the design team in client meetings.</span></li>\n<li><span>Participate in or lead data validation activities before and after go-live.</span></li>\n<li><span>Conduct hands-on clinical and external data review/reconciliation as needed.</span></li>\n<li><span>Contribute to internal guidance documentation and process improvement initiatives.</span></li>\n<li><span>Support development and review of departmental SOPs.</span></li>\n<li><span>Mentor, supervise, and train</span><span> junior team members and peers as needed.</span></li>\n</ul>\n<p> </p>\n<p><span style=\"font-family: 'Segoe UI Emoji',sans-serif;\"> </span></p>\n<p>Apply Now!<br>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.</p>",
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