Study Delivery Specialist

ICON

Multiple Locations
Clinical trial site coordination
Regulatory compliance with gcp
Cross-functional team collaboration
As a Site Management Associate II at ICON, you will play a vital role in supporting the management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines

Job Summary

  • As a Site Management Associate II at ICON, you will play a vital role in supporting the management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
  • ICON offers a range of additional benefits focused on well-being and work-life balance, including various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.
  • ICON is committed to providing an inclusive and accessible environment for all candidates and ensures equal consideration for employment without discrimination or harassment.

Matching Summary

As a Site Management Associate II at ICON, you will play a vital role in supporting the management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

Skills & Requirements

Must-have

  • clinical trial site coordination
  • regulatory compliance with GCP
  • cross-functional team collaboration
  • site performance tracking and reporting
  • stakeholder management and communication

Nice-to-have

  • experience with global project management
  • knowledge of eTMF and CTMS
  • advanced Microsoft Excel skills
  • mentoring junior staff
  • inclusive and diverse work culture

Key Requirements

  • Life Science degree
  • 1+ years clinical trial experience
  • fluent English
  • experience supporting global cross-functional teams
  • knowledge of clinical trial management systems

Work Rights

Not specified

Tailored Resume

Cover Letter