EDC Developer / Programmer

Get AI-powered advice on this job and more exclusive features.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.Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical Programmer. You will be responsible for administration of EDC Database including evaluation, analysis, design and/ or recommendations to achieve goals and excellent results in a fast-paced, ever-changing environment.This is a full time, remote opportunity, but may travel for training and key meetings.As an EDC Database Developer, 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.ResponsibilitiesServe 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 projectsPerform EDC edit check programming for assigned projects based on edit check specifications for both simple and complex edit checksCreate 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 scriptsProgram 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 standardsAssist with the validation of upgrades to hardware/ software including validation documentation development, review and executionMaintain global clinical trial database standards (CDISC)RequirementsBachelor's degree in a related field preferred3 years of clinical data management experienceAbility to program using SQL requiredExperience with EDC systems (i.e. Veeva CDMS, Medidata RAVE, etc.)Experience with Veeva EDC and Veeva CDB preferredProficient computer skills with understanding of clinical systems and data administrationMust be organized, an effective written and oral communicatorMust have the ability to multi-task, within a fast-paced environment, and build strong relationshipsCelerion Values: Integrity Trust Teamwork RespectCelerion 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, protected veteran status, or disability.Seniority levelMid-Senior levelEmployment typeContractJob functionEngineering and Information TechnologyIndustriesBiotechnology Research, Pharmaceutical Manufacturing, and Research ServicesJ-18808-Ljbffr Celerion