EDC Clinical Trial Designer
ICON · Livingston, UK
The apply link worked recently (not employer-confirmed).
Role summary
This role involves designing electronic data capture forms and clinical trial databases using tools such as Oracle InForm or Veeva CDMS. The successful candidate will manage data collection requirements, create annotated study documentation, conduct validation testing, and collaborate with study teams to deliver high-quality eCRF solutions. A BA/BS degree and minimum 2 years of clinical data management experience are required.
What they're looking for
- Bachelor's degree in relevant field or equivalent clinical data management experience
- Minimum 2 years of clinical data management experience with electronic data capture systems
- Strong oral and written communication and presentation abilities
- Meticulous attention to detail with commitment to quality and minimal errors
- Ability to manage multiple projects and deliverables in fast-paced environment
- Preferred: clinical trial planning and management experience in biopharmaceutical industry
- Preferred: familiarity with CDISC/CDASH/SDTM standards and clinical research processes
What you'll be doing
- Design and develop high-quality eCRF forms using Oracle InForm/Central Designer or Veeva CDMS/Studio
- Analyze data collection requirements from protocol and study team input to inform form design
- Develop test steps, conduct quality control, and validate study and schedule designs
- Create annotated study books and work with form libraries to support trial implementation
- Communicate project scope, timelines, and requirements to study team members through meetings
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.