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EDC Developer / Programmer

1 month, 3 weeks ago
United States
Full-time
Mid Level
Software Engineer
Software Development
SQL
Apply Now
Celerion

Celerion

Celerion is a pioneer in early clinical research, offering Applied Translational Medicine services worldwide to expedite drug development processes.

Pharmaceuticals
251-1K
Founded 2010
View All Jobs 5

Description

  • Administer EDC databases and support study setup from protocol and requirements review through implementation and maintenance.
  • Design and build electronic case report forms (eCRFs) and corresponding edit checks for assigned projects.
  • Program EDC edit checks based on specifications, including both simple and complex logic.
  • Create test data and prepare test environments to verify screen design and edit check functionality before UAT.
  • Coordinate project team members and execute test scripts during validation and testing activities.
  • Configure listings and reports using clinical reporting tools such as Veeva Clinical Database (CDB).
  • Serve as a subject matter expert for Veeva Clinical Data Management Suite (CDMS), including Veeva EDC and Veeva CDB.
  • Support secure database imports from vendor transfers using Celerion data transfer standards.
  • Assist with validation of hardware and software upgrades, including documentation, review, and execution.
  • Set up interface connections between EDC and other systems and troubleshoot or escalate technical issues with vendors.

Requirements

  • Bachelor’s degree in a related field preferred.
  • 3 years of clinical data management experience.
  • Ability to program using SQL.
  • Experience with EDC systems such as Veeva CDMS or Medidata RAVE.
  • Experience with Veeva EDC and Veeva CDB preferred.
  • Proficient computer skills with understanding of clinical systems and data administration.
  • Strong organizational skills and effective written and oral communication.
  • Ability to multitask in a fast-paced environment and build strong working relationships.
  • Ability to travel for training and key meetings.
  • Knowledge of global clinical trial database standards such as CDISC.

Interested in this position?

Apply directly on the company website

Apply Now

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