EDC Developer / Programmer
C
CelerionClinical Research
USAFull-TimeMiddle
Salary not disclosed
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Job Details
- Experience
- 3 years of clinical data management experience
- Required Skills
- SQL
Requirements
- Bachelor’s degree in a related field preferred.
- 3 years of clinical data management experience.
- Ability to program using SQL required.
- Experience with EDC systems (i.e. Veeva CDMS, Medidata RAVE, etc.).
- Experience with Veeva EDC and Veeva CDB preferred.
- Proficient computer skills with understanding of clinical systems and data administration.
- Must be organized and an effective written and oral communicator.
- Ability to multi-task within a fast-paced environment and build strong relationships.
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 based on specifications for both simple and complex edit checks.
- Create test data to verify screen design and edit check programming prior 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).
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