Senior Associate, Pharmacovigilance - Japan - Remote

Worldwide Clinical Trials

Japan
Minimum 5 years pharmacovigilance experience
Bachelor's degree in science or nursing
Fluent written and verbal english
The role involves authoring safety management plans and reviewing safety events from around the world to ensure drug safety

Job Summary

  • The role involves authoring safety management plans and reviewing safety events from around the world to ensure drug safety.
  • Candidates must have at least five years of pre-approval clinical trials experience within the pharmacovigilance field.
  • The company fosters a diverse and inclusive environment where professionals are encouraged to be themselves and do their best work.

Matching Summary

The role involves authoring safety management plans and reviewing safety events from around the world to ensure drug safety.

Skills & Requirements

Must-have

  • Minimum 5 years pharmacovigilance experience
  • Bachelor's degree in science or nursing
  • Fluent written and verbal English
  • Review incoming SAE data for accuracy
  • Generate queries for missing information
  • Perform QC of SAEs processed by others

Nice-to-have

  • Ability to work independently in matrix teams
  • Positive attitude with diplomatic interaction skills
  • Willingness for limited domestic and international travel
  • Experience mentoring new PV staff
  • Strong organizational skills for competing priorities

Key Requirements

  • 5+ years pharmacovigilance experience
  • Bachelor's degree in science-related field
  • Fluency in English required

Work Rights

Not specified

Tailored Resume

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