Clinical Database Programmer

This is a fully remote position, open to applicants in United States.

📋 Description

• Oversee EDC databases for clinical trial projects contracted by clients

• Assess protocols and project requirements

• Create and develop electronic case report forms (eCRFs) along with necessary edits

• Diagnose and escalate system issues to the appropriate stakeholders

• Engage technically with vendors supporting the application

• Offer expert advice on study setup design, development, validation, implementation, and maintenance

• Manage the deployment of EDC trials

• Establish interface connections between EDC and other systems

• Conduct eCRF design and EDC build programming

• Program both simple and complex EDC edit checks

• Generate test data to validate screen design and edit-check programming prior to User Acceptance Testing (UAT)

• Configure test environments and coordinate project team members in executing test scripts

• Set up listings and reports utilizing Veeva Clinical Database and clinical reporting tools

• Ensure secure and high-integrity database imports from vendor transfers following Celerion data transfer standards

• Support hardware/software upgrade validation and associated documentation

• Uphold global clinical trial database standards (CDISC)

⛳️ Requirements

• Bachelor's degree in a relevant field is preferred

• A minimum of 3 years of experience in clinical data management

• Proficiency in programming with SQL is required

• Familiarity with Veeva EDC and Veeva CDB

• Strong computer skills and a solid understanding of clinical systems and data administration

• Organized and effective in both written and verbal communication

• Capable of multitasking in a dynamic environment and fostering strong relationships

🏝️ Benefits

• Opportunities for travel related to training and important meetings