Site Specialist Ii (study Start Up Associate Ii)

ICON Clinical Research, LP

Taipei, Taiwan
Hybrid
Icon sops/wps knowledge
Ich/gcp adherence
Regulatory country regulations
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization focused on fostering an inclusive environment driving innovation and excellence.
  • The role involves supporting site activation by collecting, reviewing, and assembling regulatory submission packages, ensuring accuracy and completeness of critical documents, and coordinating translations.
  • ICON offers competitive salaries and a range of benefits designed for well-being and work-life balance, including annual leave, health insurance, retirement planning, and a global employee assistance program.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization focused on fostering an inclusive environment driving innovation and excellence.

Skills & Requirements

Must-have

  • ICON SOPs/WPs knowledge
  • ICH/GCP adherence
  • regulatory country regulations
  • study start-up packages
  • Critical Document Package assembly
  • TMF document QC review

Nice-to-have

  • inclusive environment
  • foster innovation and excellence
  • risk identification and mitigation

Key Requirements

  • Proficient knowledge of ICON SOPs/WPs
  • Proficient knowledge of ICH/GCP
  • Proficient knowledge of applicable country regulations/guidelines
  • Proficient knowledge of ICON systems

Work Rights

Not specified

Tailored Resume

Cover Letter