Clinical Db Designer

IQVIA UK

Bangalore, India
Study protocol interpretation
Ecrf design and update
Edit specification document creation
Responsible for study design, edit specifications, and system configurations, ensuring quality and timely delivery of assigned study design components

Job Summary

  • Responsible for study design, edit specifications, and system configurations, ensuring quality and timely delivery of assigned study design components.
  • Key responsibilities include interpreting study protocols, designing and updating eCRFs, creating edit specifications, and generating specifications for EDC build components.
  • The role involves attending various meetings, facilitating reviews, designing databases for specific data collection, communicating project risks, and escalating quality issues.

Matching Summary

Responsible for study design, edit specifications, and system configurations, ensuring quality and timely delivery of assigned study design components.

Skills & Requirements

Must-have

  • study protocol interpretation
  • eCRF design and update
  • edit specification document creation
  • EDC build component specification
  • InForm database design

Nice-to-have

  • collaboration with project stakeholders
  • risk communication to Data Team Lead
  • quality issue escalation
  • project-specific training completion

Key Requirements

  • 0-2 years core Technical designer experience
  • 5+ years total experience
  • Bachelor's Degree in Science/Computer science/Information Technology or Bachelor in Technology

Work Rights

Not specified

Tailored Resume

Cover Letter