Veeva Clinical Database Programmer

In this role you will:

• Serve as a subject matter expert in Veeva Clinical Data Management Suite (CDMS), including Veeva Electronic Data Capture (EDC) and Veeva Clinical Database (CDB)
• Perform all activities related to eCRF design and EDC build programming for assigned projects
• Perform EDC edit check programming for assigned projects based on edit check specifications for both simple and complex edit checks
• Create test data to verify both screen design and edit check programming prior to deploying to User Acceptance Testing (UAT)
• Set up test environments and coordinate project team members for execution of test scripts
• Program and configure listings and reports using clinical reporting tools such as Veeva Clinical Database (CDB)
• Ensure secure and high-integrity database imports from vendor transfers using Celerion data transfer standards
• Assist with the validation of upgrades to hardware/ software including validation documentation development, review and execution.
• Maintain global clinical trial database standards (CDISC)

Requirements:

• Bachelor’s degree in a related field preferred
• 3 years of clinical data management experience
• Ability to program using SQL required
• Experience with Veeva EDC and Veeva CDB 
• Proficient computer skills with understanding of clinical systems and data administration
• Must be organized, an effective written and oral communicator
• Must have the ability to multi-task, within a fast-paced environment, and build strong relationships 
 
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