{"schemaVersion":"jobsearcher.job.v1","id":"b437c19a686e09774f030e30","url":"https://jobsearcher.com/jobs/b437c19a686e09774f030e30","canonicalUrl":"https://jobsearcher.com/jobs/b437c19a686e09774f030e30","title":"Veeva Clinical Database Programmer","description":"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.\n\nAre you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!\nWe 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.\nThis is a full-time, remote opportunity, but you may travel for training and key meetings.\nAs 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.\nIn this role you will:\nServe as a subject matter expert in Veeva Clinical Data Management Suite (CDMS), including Veeva Electronic Data Capture (EDC) and Veeva Clinical Database (CDB)\nPerform all activities related to eCRF design and EDC build programming for assigned projects\nPerform EDC edit check programming for assigned projects based on edit check specifications for both simple and complex edit checks\nCreate test data to verify both screen design and edit check programming prior to deploying to User Acceptance Testing (UAT)\nSet up test environments and coordinate project team members for execution of test scripts\nProgram and configure listings and reports using clinical reporting tools such as Veeva Clinical Database (CDB)\nEnsure secure and high-integrity database imports from vendor transfers using Celerion data transfer standards\nAssist with the validation of upgrades to hardware/ software including validation documentation development, review and execution.\nMaintain global clinical trial database standards (CDISC)\nRequirements:\nBachelor’s degree in a related field preferred\n3 years of clinical data management experience\nAbility to program using SQL required\nExperience with Veeva EDC and Veeva CDB\nProficient computer skills with understanding of clinical systems and data administration\nMust be organized, an effective written and oral communicator\nMust have the ability to multi-task, within a fast-paced environment, and build strong relationships\n#LI-Remote\nCelerion Values: Integrity Trust Teamwork Respect\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n\nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n\nWe may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.","company":"Celerion","rawCompany":"celerion","city":"Remote","state":"OR","isRemote":false,"isActive":false,"createdAt":"2026-08-13T14:36:41.112Z","occupations":[{"code":"15-2051.02","title":"Clinical Data Managers","slug":"clinical-data-managers"},{"code":"15-1252.00","title":"Software Developers","slug":"software-developers"},{"code":"15-1251.00","title":"Computer Programmers","slug":"computer-programmers"}],"industries":[{"code":"541511","title":"Custom Computer Programming Services","slug":"custom-computer-programming-services"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"541512","title":"Computer Systems Design Services","slug":"computer-systems-design-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Veeva Clinical Database Programmer","description":"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.\n\nAre you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!\nWe 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.\nThis is a full-time, remote opportunity, but you may travel for training and key meetings.\nAs 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.\nIn this role you will:\nServe as a subject matter expert in Veeva Clinical Data Management Suite (CDMS), including Veeva Electronic Data Capture (EDC) and Veeva Clinical Database (CDB)\nPerform all activities related to eCRF design and EDC build programming for assigned projects\nPerform EDC edit check programming for assigned projects based on edit check specifications for both simple and complex edit checks\nCreate test data to verify both screen design and edit check programming prior to deploying to User Acceptance Testing (UAT)\nSet up test environments and coordinate project team members for execution of test scripts\nProgram and configure listings and reports using clinical reporting tools such as Veeva Clinical Database (CDB)\nEnsure secure and high-integrity database imports from vendor transfers using Celerion data transfer standards\nAssist with the validation of upgrades to hardware/ software including validation documentation development, review and execution.\nMaintain global clinical trial database standards (CDISC)\nRequirements:\nBachelor’s degree in a related field preferred\n3 years of clinical data management experience\nAbility to program using SQL required\nExperience with Veeva EDC and Veeva CDB\nProficient computer skills with understanding of clinical systems and data administration\nMust be organized, an effective written and oral communicator\nMust have the ability to multi-task, within a fast-paced environment, and build strong relationships\n#LI-Remote\nCelerion Values: Integrity Trust Teamwork Respect\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n\nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n\nWe may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.","datePosted":"2026-08-13T14:36:41.112Z","dateModified":"2026-08-13T14:36:41.112Z","hiringOrganization":{"@type":"Organization","name":"Celerion","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Remote","addressRegion":"OR","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"b437c19a686e09774f030e30"},"url":"https://jobsearcher.com/jobs/b437c19a686e09774f030e30"}}