We 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.
This is a
full-time, remote opportunity, but you may travel for training and key meetings.
As 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.
In this role you will:- 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)
Requirements:- Bachelor's degree in a related field preferred
- 3 years of clinical data management experience
- Ability to program using SQL required
- Experience with Veeva EDC and Veeva CDB
- 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
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Celerion Values: Integrity Trust Teamwork Respect
