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.
