Clinical Db Designer

IQVIA

Kochi, 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 functions include interpreting study protocols, designing and updating eCRFs, creating edit specifications, and generating specifications for EDC build components.
  • Attend and present at various meetings including Pre-Design, Screen Review, Unblinded Data Review, and Internal Design Review, facilitating discussions on edit specifications.

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 specifications
  • InForm database design

Nice-to-have

  • Project risk communication
  • Quality issue escalation
  • Project-specific training completion
  • Standard Operating Procedures adherence

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter