Business Operations Associate - Site And Ssu Specialist

ICON

Tokyo, Japan
Regulatory document preparation and submission
Clinical trial study start-up activities
Stakeholder coordination for approvals
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
  • The role involves leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.
  • ICON offers competitive salary and a range of 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 fostering an inclusive environment driving innovation and excellence.

Skills & Requirements

Must-have

  • Regulatory document preparation and submission
  • Clinical trial study start-up activities
  • Stakeholder coordination for approvals
  • Regulatory compliance management
  • Project management skills
  • Cross-functional team collaboration

Nice-to-have

  • Process improvement initiatives
  • Strong organizational skills
  • Excellent communication and interpersonal skills
  • Inclusive and diverse work environment

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Minimum 2 years clinical research or regulatory affairs experience
  • Experience in study start-up activities
  • Strong understanding of ICH-GCP and local regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter