Clinical Supply Chain Manager, Home-office

IQVIA UK

3-5 years clinical trials experience
3-5 years clinical supply chain management
Interpret clinical trial protocols
This role involves shaping and driving the end-to-end supply strategy for new clinical trials by translating complex study protocols into smart kit designs

Job Summary

  • This role involves shaping and driving the end-to-end supply strategy for new clinical trials by translating complex study protocols into smart kit designs.
  • The successful candidate will collaborate with internal teams and external partners to ensure seamless study execution while maintaining the highest quality standards.
  • Key responsibilities include creating demand forecasts, managing packaging campaigns, and overseeing temperature excursion processes to ensure timely delivery of trial materials.

Matching Summary

This role involves shaping and driving the end-to-end supply strategy for new clinical trials by translating complex study protocols into smart kit designs.

Skills & Requirements

Must-have

  • 3-5 years clinical trials experience
  • 3-5 years clinical supply chain management
  • Interpret clinical trial protocols
  • Create master English label text
  • Manage Interactive Response Technology systems
  • Conduct risk management assessments

Nice-to-have

  • Bachelor's degree in science or business
  • Strong Microsoft Office skills
  • Effective stakeholder relationship building
  • Proactive independent problem solving
  • Experience with Annex 13 regulations

Key Requirements

  • Bachelor's Degree (Preferred)
  • 3-5 Years industry experience in Clinical Trials
  • 3-5 Years experience in Clinical Supply Chain Management
  • Proficient in English language
  • Not eligible for UK visa sponsorship

Work Rights

Must have right to work in UK without sponsorship

Tailored Resume

Cover Letter