Veeva Clinical Database Programmer

C
CelerionClinical Research
Remote - USFull-TimeMiddle
Salary not disclosed
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Job Details

Experience
3 years
Required Skills
SQL

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 and an effective written and oral communicator
  • Ability to multi-task in a fast-paced environment
  • Ability to build strong professional relationships

Responsibilities

  • 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
  • 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)
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