Site Specialist Ii (study Start Up Associate Ii)

ICON

Taipei, Taiwan
Hybrid
Proficient knowledge of icon sops/wps
Ich/gcp and applicable country regulations
Collect, review, organize submission packages
ICON plc is a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment that drives innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment that drives innovation and excellence.
  • Responsibilities include 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, a range of benefits focused on well-being and work-life balance, including various annual leave, health insurance, retirement planning, and global employee assistance programs.

Matching Summary

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

Skills & Requirements

Must-have

  • Proficient knowledge of ICON SOPs/WPs
  • ICH/GCP and applicable country regulations
  • Collect, review, organize submission packages
  • Assemble Critical Document Package (CDP)
  • Timely update tracking tools
  • Coordination of translations
  • Progress data entry into tracking systems

Nice-to-have

  • Foster inclusive environment
  • Drive innovation and excellence
  • Accountability and Delivery
  • Collaboration, Partnership and Integrity
  • Risk identification and mitigation

Key Requirements

  • Proficient knowledge of ICON systems
  • Experience with site activation process
  • Quality Control (QC) review of files

Work Rights

Not specified

Tailored Resume

Cover Letter