eCOA Database Developer

Summary

Join Celerion as a full-time remote Veeva eCOA Database Developer, contributing to swift and exceptional clinical research through translational medicine. You will be responsible for building and administering Celerion databases within the eCOA environment, ensuring data acquisition, quality checking, and reporting meet project deliverables, timelines, and budgets. This role involves collaborating with various teams, including Clinical Data Managers, Biostatisticians, Clinical and Project Management staff, and Sponsors. Travel is required domestically and/or internationally for this position.

Requirements

• 3 years or equivalent experience in clinical research using eCOA-like systems to collect data and report
• Excellent computer skills with understanding of clinical systems and data administration
• Ability to program using appropriate languages such as JSON
• Ability to organize and manage multiple concurrent priorities required
• Excllent oral and written communication required
• Excellent organizational skills required
• Problem solving skills required

Responsibilities

• Perform all activities related to eCOA design and build programming for assigned projects including preparing eCOA specifications and any special licensing that is required for the survey/questionnaire
• Coordinate licensing if needed for any survey/questionnaires
• Create test data / scripts to test both the screen design and validation checks
• Create, build and maintain programmatic/functional template libraries and utlilize templates as necessary to speed development
• Perform ad-hoc programming support such as listing and reports creation using clinical reporting tools within the eCOA
• Provide timely support to the study team on all programming matters according to the project plan and programming specification using internal, standards and guidelines
• Ensure completeness, correctness and consistency of eCOA design, data extracts and listings, and clinical data and data structure
• Maintain global clinical trial database standards (CDISC)
• Troubleshoot problems on eCOA system, escalate to IT and vendor as needed
• Manage the deployment of eCOA trials and setup interface connections between eCOA and other systems, including complex deployments and study specific configurations
• Contribute to special projects to meet the business needs from internal and external groups
• Author and review procedures and work instructions
• Coordinate upgrades of hardware/software including validation documentation development, review and execution
• Setup test system environments and coordinate project team members for execution of test scripts
• Create validation documentation according to Celerion SOPs and move these documents through the completion, review and approval process

Preferred Qualifications

Bachelor’s degree in related field preferred