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Expect scenarios on Veeva Vault/CDMS builds, edit-check design, migration and amendment handling, GxP documentation, and how you partner with DM and stats under tight study go-live dates. Be ready to walk through a past database build end to end.
Strong fit if you have hands-on Veeva or clinical EDC programming in a CRO/pharma setting and work well fully remote across U.S. teams. Thin public culture signal—ownership and capacity news do not substitute for direct employee feedback.
As a remote Veeva Clinical Database Programmer at Celerion, a typical day centers on building and maintaining clinical databases in Veeva (or related EDC) for early- and late-phase studies: CRF design, edit checks, listings, query logic, and UAT support with data managers and biostats. You resolve data issues, document specs, and keep builds aligned with protocol amendments under CRO timelines.
Yes—the listing is remote within the United States.
It provides clinical research and related drug-development services; recent news also notes bioanalytical lab growth in Zurich.
No cert family or cost list was provided for this occupation; emphasize Veeva/EDC and clinical data experience instead.
Website: celerion.com
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Veeva Clinical Database Programmer at Celerion - Remote (US) About This Position This is a full-time, remote opportunity where you will build and administer EDC trials for client-contracted projects. Responsibilities include protocol/requirements evaluation, electronic case report form (eCRF) design and build with corresponding edits, technical interaction with vendors, troubleshooting, escalation of problems, expert guidance on study setup, deployment of EDC trials, and management of interface connections between EDC and other systems. Day-to-Day Responsibilities Evaluation, analysis, and design of EDC database to achieve goals and excellent results in a fast-paced environment Technical interaction with vendors for support and troubleshooting Escalation of system problems to appropriate partners Expert guidance on the design, development, validation, implementation, and maintenance of study setup Deployment of EDC trials and management of interface connections between EDC and other systems Who We're Looking For We are seeking a performance-oriented, innovative, and self-motivated team player with experience in the administration of EDC database. You should be able to handle fast-paced, ever-changing environments and have technical interaction skills. This role will involve collaboration with vendors and troubleshooting/escalation of problems on systems. About the Company Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. We are looking for an opportunity to support a business creating life-saving treatments. Next Steps To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.
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