Site Specialist Ii

ICON Clinical Research, LP

Beijing, China
On-site
Regulatory document preparation
Study initiation compliance
Stakeholder coordination
ICON plc is a world-leading healthcare intelligence and clinical research organization

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization.
  • You will play a pivotal role in leading the initiation of clinical trials.
  • Our benefits are designed to be competitive and focused on well-being and work-life balance.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization.

Skills & Requirements

Must-have

  • Regulatory document preparation
  • Study initiation compliance
  • Stakeholder coordination

Nice-to-have

  • Process improvement initiatives
  • Cross-functional team collaboration
  • Strong organizational skills

Key Requirements

  • Bachelor's degree in life sciences
  • Minimum of 4 years in clinical research
  • Strong understanding of regulatory guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter