Drug Safety Associate

ICON Clinical Research, LP

South Korea
Competitive salary; not specified; various annual ...
Fully remote
Adverse event report management
Safety system data entry
Regulatory reporting submission
This role is pivotal in ensuring drug safety by managing the collection, processing, and reporting of adverse events from various sources including clinical trials and spontaneous reports

Job Summary

  • This role is pivotal in ensuring drug safety by managing the collection, processing, and reporting of adverse events from various sources including clinical trials and spontaneous reports.
  • The successful candidate will ensure quality and consistency across multiple projects while supporting the development of training courses and standard operating procedures.
  • ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a commitment to an inclusive workplace culture.

Matching Summary

This role is pivotal in ensuring drug safety by managing the collection, processing, and reporting of adverse events from various sources including clinical trials and spontaneous reports.

Salary

Competitive salary; Not specified; Various annual leave, health insurance, retirement planning, and global employee assistance program

Skills & Requirements

Must-have

  • Adverse event report management
  • Safety system data entry
  • Regulatory reporting submission
  • ICSR processing and tracking
  • Source document transcription

Nice-to-have

  • Training course development support
  • SOP creation and maintenance
  • Global regulatory intelligence activities
  • Client license partner collaboration
  • Inclusive team environment participation

Key Requirements

  • 1 to 1.5 years related experience
  • Undergraduate degree in life science or healthcare
  • Advanced knowledge of Pharmacovigilance regulations

Work Rights

Not specified

Tailored Resume

Cover Letter