Clinical Db Designer

IQVIA UK

Kochi, India
Study design
Ecrf design
Edit specification document
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 requires attending various meetings such as Pre-Design, Screen Review, Unblinded Data Review, and Internal Design Review, and facilitating Edit Specification Review Meetings.

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 design
  • eCRF design
  • edit specification document
  • EDC build specifications
  • InForm database design

Nice-to-have

  • collaboration with stakeholders
  • risk communication
  • quality issue escalation
  • project training completion

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter