Database Programmer

Job Description

Key Responsibilities

• Perform post-production changes to live clinical studies in Zelta EDC
• Conduct impact analysis for database updates and change requests
• Review and interpret study specifications
• Implement and update CRFs (Case Report Forms)
• Manage visit mapping and study configuration changes
• Develop and maintain edit checks/validation rules
• Ensure accurate documentation and compliance with processes
• Participate in process reviews and continuous improvement initiatives

Requirements

• Proven experience as a Database Programmer in clinical trials
• Strong hands-on experience with Merative Zelta EDC (essential)
• Solid understanding of clinical data management processes
• Experience with post-production database changes
• Attention to detail and ability to assess impact across live studies
• Strong communication and documentation skills

Nice to Have

• Experience working in a CRO or sponsor environment
• Familiarity with regulatory standards (GCP, 21 CFR Part 11)

Are you interested in this position?

Apply by clicking on the “Apply Now” button below!

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