Associate Clinical System Designer
ICON
ICON seeks an Associate Clinical System Designer to support the design and implementation of clinical data systems for trial execution. The role involves developing CRF specifications, technical documentation, and quality control activities across multiple locations in North America, Mexico, and Colombia.
Responsibilities
- Develop and assist with CRF screens, Edit Check, and Dynamic Check specification documents
- Create technical specifications for data validation, analytics, and custom output programs
- Copy and modify CRFs from standard libraries under instruction
- Track issues and communicate risks affecting project timelines, scope, or budget
- Support eCRF specification reviews and perform quality control peer reviews
Requirements
- 6+ months experience designing and implementing clinical systems in clinical research
- Expertise in data analysis, interpretation, or database development
- Proficiency with Medidata Rave and/or Veeva EDC platforms
- Functional knowledge of CRF design tools and clinical trial protocol interpretation
- Excellent written and verbal communication skills
- Bachelor's Degree in a relevant field
Vacancy posted 21 hours ago
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