Veeva Clinical Database Programmer

Celerion

6d • Remote

About The Position

Celerion is seeking a performance-oriented, innovative, and self-motivated team player to join their Clinical Data Sciences team as a full-time Veeva Clinical Database Programmer. This role is responsible for the administration of EDC databases, including evaluation, analysis, design, and recommendations to achieve goals in a fast-paced, ever-changing environment. This is a full-time, remote opportunity, with potential travel for training and key meetings. The programmer will build and administer EDC trials for client-contracted projects, including protocol/requirements evaluation, eCRF design and build with corresponding edits. The role involves technical interaction with vendors supporting applications, troubleshooting and escalating problems, and providing expert guidance on study set-up, development, validation, implementation, and maintenance. Additionally, the role will manage the deployment of EDC trials and set up interface connections between EDC and other systems.

Requirements

• 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

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 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)

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level