(senior) Site Specialist

ICON

Taipei, Taiwan
Hybrid
Proficient knowledge of icon sops/wps
Experience with ich/gcp guidelines
Site activation process management
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation, excellence, and fostering an inclusive environment

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation, excellence, and fostering an inclusive environment.
  • The role involves coordinating site activation activities, ensuring regulatory compliance, and supporting study performance through collaboration with site partners and internal stakeholders.
  • ICON offers competitive benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation, excellence, and fostering an inclusive environment.

Skills & Requirements

Must-have

  • Proficient knowledge of ICON SOPs/WPs
  • Experience with ICH/GCP guidelines
  • Site activation process management
  • Regulatory submission package assembly
  • Trial Master File document quality control
  • Use of internal tracking tools for site activation

Nice-to-have

  • Collaborative team work
  • Training and onboarding junior specialists
  • Risk identification and mitigation
  • Inclusive and diverse work culture
  • Office hybrid work environment

Key Requirements

  • Knowledge of ICH/GCP and country regulations
  • Experience with regulatory submission processes
  • Ability to perform quality control reviews
  • Experience in clinical trial site activation
  • Familiarity with Trial Master File documentation

Work Rights

Not specified

Tailored Resume

Cover Letter