Clinical Db Designer

IQVIA UK

Interpret study protocols
Design and update ecrf
Create edit specification document
The Clinical Database Designer is responsible for interpreting study protocols to design and update electronic Case Report Forms (eCRFs)

Job Summary

  • The Clinical Database Designer is responsible for interpreting study protocols to design and update electronic Case Report Forms (eCRFs).
  • This role requires creating detailed Edit Specification Documents and generating specifications for EDC build components within the InForm system.
  • The incumbent must ensure timely delivery of study design components while managing quality issues and communicating risks to the Data Team Lead.

Matching Summary

The Clinical Database Designer is responsible for interpreting study protocols to design and update electronic Case Report Forms (eCRFs).

Skills & Requirements

Must-have

  • Interpret study protocols
  • Design and update eCRF
  • Create Edit Specification Document
  • Generate EDC build specifications
  • Manage InForm database rights and roles

Nice-to-have

  • Facilitate internal review meetings
  • Communicate project risks effectively
  • Collaborate with project stakeholders

Key Requirements

  • Bachelor's Degree in Science, Computer Science, IT, or Technology
  • 0-2 years relevant core Technical designer experience
  • Total experience of 5+ years required

Work Rights

Not specified

Tailored Resume

Cover Letter