Global Clinical Delivery Manager

ICON

Minimum of 5 years of experience in clinical research
Excellent knowledge of ich-gcp
Vendor management experience
As a Global Study Manager at ICON, you will play a pivotal role in supporting the coordination and management of clinical trials globally

Job Summary

  • As a Global Study Manager at ICON, you will play a pivotal role in supporting the coordination and management of clinical trials globally.
  • GSM is responsible for monitoring study conduct and progress, identifying, resolving and escalating risks/issues which may impact delivery.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance.

Matching Summary

As a Global Study Manager at ICON, you will play a pivotal role in supporting the coordination and management of clinical trials globally.

Skills & Requirements

Must-have

  • Minimum of 5 years of experience in clinical research
  • Excellent knowledge of ICH-GCP
  • Vendor management experience
  • Global experience

Nice-to-have

  • Strong project management skills
  • Good leadership skills
  • Excellent communication and relationship building skills

Key Requirements

  • Bachelor's degree in a scientific or related field
  • 1-2 years working as an Associate Project Manager
  • Well familiar with key systems used in clinical trial delivery

Work Rights

Not specified

Tailored Resume

Cover Letter