EDC Developer / Programmer

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
• Absorb and 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 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, an effective written and oral communicator
• Must have the ability to multi-task, within a fast-paced environment, and build strong relationships

Qualifications

Celerion Values: Integrity Trust Teamwork Respect

Celerion 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.