SR Clinical Data Systems Designer

hace 5 días

Medellín, Antioquia, Colombia Yuxi Global A tiempo completo
Company Description

Yuxi Global (powered by Veritas Automata) has been a leading force in empowering Life Sciences companies to achieve their digital goals since 2005.

We specialize in providing comprehensive solutions, including turnkey enterprise-grade application development, managed development teams, staff augmentation, and strategic consulting via our Veritas Automata Services Team. With headquarters in the United States and a team of over 150 skilled IT professionals located throughout North and South America, including the United States, Colombia, Mexico, Brazil, and Costa Rica, we are well-positioned to meet the unique requirements of our clients.

Having partnered with nearly 300 clients, Yuxi Global has played a crucial role in advancing digital solutions for companies in life sciences. Utilizing cutting-edge technologies such as Microsoft Azure, PowerBI, .Net Custom development, Node.JS, React, and UX/UI design, we deliver impactful solutions that drive business growth and captivate audiences.

Job Description

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.
Qualifications

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.
Additional Information

Integración vida-trabajo: Apoyamos el equilibrio vida-trabajo y la oportunidad de crear una mayor sinergia entre el trabajo; hogar; familia; y bienestar personal.

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