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# Veeva Clinical Database Programmer

- **Company:** Celerion
- **Location:** Poland, ME, United States (Remote available)
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Clinical Data Management, Clinical Data Repository, Databases, Data Transmissions, Electronic Data Capture, SQL Databases, Test Data, Test Scripts, Build Management, Data Management, Tools for Reporting, Veeva
- **Published:** August 7, 2026
- **Apply:** https://www.workingnomads.com/job/go/1777445/

## About the Role

We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Veeva Clinical Database Programmer. You will be responsible for the administration of EDC database, including evaluation, analysis, design and/ or recommendations to achieve goals and excellent results in a fast-paced, ever-changing environment., * 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

#LI-Remote

Celerion Values: Integrity Trust Teamwork Respect

## Description

As a Veeva Clinical Database Programmer, you will build and administer EDC trials for client-contracted projects, including protocol/requirements evaluation, electronic case report form (eCRF) design and build with corresponding edits. This role will have technical interaction with vendors that are supporting the applications and troubleshoot/ escalate problems on systems to appropriate partners. This role will provide expert guidance to the design, development, validation, implementation and maintenance of study set-up. Additionally, this role will manage the deployment of EDC trials and set up interface connections between EDC and other systems.
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)


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