Note: The job is a remote job and is open to candidates in USA. Celerion is committed to swift, exceptional clinical research through translational medicine. They are seeking a performance-oriented and innovative EDC Database Developer to join their Clinical Data Sciences team, responsible for the administration of EDC databases and ensuring high-quality data management for clinical trials.
Responsibilities
- 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)
Skills
- 3 years of clinical data management experience
- Ability to program using SQL required
- Experience with EDC systems (i.e. Veeva CDMS, Medidata RAVE, etc.)
- 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
- Bachelor's degree in a related field preferred
- Experience with Veeva EDC and Veeva CDB preferred
Company Overview
Company H1B Sponsorship