Celerion
Veeva Clinical Database Programmer
Remote - US (Remote)full-timemidAdded today
About this role
Celerion seeks a Veeva Clinical Database Programmer to design, build, and administer electronic data capture (EDC) systems for clinical trials. You'll manage database architecture, eCRF design, system validation, and vendor coordination in a remote, fast-paced research environment.
What you'll do
- Design and build electronic case report forms (eCRFs) with appropriate validation edits
- Evaluate protocols and technical requirements to inform EDC database architecture
- Administer and maintain EDC trial systems throughout study lifecycle
- Coordinate with third-party vendors to troubleshoot system issues and escalate problems
- Manage EDC deployment and configure interface connections between EDC and other systems
- Provide expert guidance on validation, implementation, and maintenance of study setups
What they're looking for
- Veeva EDC platform expertise
- Electronic data capture (EDC) system design and administration
- eCRF design and build
- Clinical trial protocol understanding
- Data validation and edit logic
- System integration and interface management
- Vendor management and technical troubleshooting
- Regulatory compliance knowledge (21 CFR Part 11)
Opens the application — the Jobs AI extension fills it for you. Set up autofill
Opens the official application on the employer’s site. No login required.
Celerion
Celerion builds electronic data capture (EDC) systems and infrastructure for clinical trials supporting drug development. The company is hiring for technical roles including database developers and system administrators who design, implement, and maintain clinical trial data systems.
- Website
- celerion.com
Likely interview questions
- Walk us through your experience designing and building eCRFs in Veeva—what complexity of edits have you implemented?
- How have you approached evaluating clinical protocols to translate requirements into EDC database specifications?