EDC Clinical Trial Developer: Build & Validate eCRF Systems

Kaztronix; Wilmington (DE); On-site; USD 90,000 - 130,000; Full time

Job summary

Kaztronix is seeking an EDC Clinical Trial Developer to design data collection tools for new trials and develop eCRF forms using Veeva CDMS/Studio. You will program edit checks, build forms, and generate complex reports via Veeva Workbench to support timely study delivery.

Responsibilities include deployment validation, study design testing, and communicating requirements to the study team. A strong data management background and CDISC knowledge are preferred.

Qualifications

• BA/BS degree in CS or related field.
• Minimum 2 years Clinical Data Management with eDC experience preferred.
• Basic programming experience required.
• SQL and/or CQL experience.
• Strong communication skills and attention to detail.
• Ability to manage multiple tasks in a fast-paced environment.
• Familiarity with CDISC/CDASH/SDTM preferred.

Responsibilities

• Design eCRF forms using Veeva Studio and develop forms workflow.
• Program basic edit checks and set up simple integrations.
• Create complex reports using Veeva Workbench and SQL.
• Validate deployments to test and live environments.
• Produce annotated study books and maintain documentation.
• Communicate scope, timelines and requirements to study teams.

Skills

Data management

Communication

Attention to detail

Project coordination

Education

BA/BS degree in CS or related field

Tools

Veeva Studio

Veeva Workbench

SQL

CQL

Job description

Kaztronix is seeking an EDC Clinical Trial Developer to design data collection tools for new trials and develop eCRF forms using Veeva CDMS/Studio. You will program edit checks, build forms, and generate complex reports via Veeva Workbench to support timely study delivery.

Responsibilities include deployment validation, study design testing, and communicating requirements to the study team. A strong data management background and CDISC knowledge are preferred.