Senior Associate, Pharmacovigilance - Japan - Remote

Worldwide Clinical Trials

Tokyo, Japan
Fully remote
Safety management plan authoring
Sae data review and entry
Regulatory reporting and submissions
Worldwide Clinical Trials is seeking a Senior Associate in Pharmacovigilance for a remote position in Japan. The ideal candidate will have extensive experience in drug safety and clinical trials, with a focus on effective communication and organization

Job Summary

  • Our Pharmacovigilance team comprises a dynamic group of individuals with extensive experience within the Drug Safety world.
  • We review safety events from all over the world and work with our clients to review, analyze, and submit to Investigators, Ethics Committees/IRBs, and Regulatory Agencies furthering clinical drug development!
  • We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

Matching Summary

Match Score: 85

Worldwide Clinical Trials is seeking a Senior Associate in Pharmacovigilance for a remote position in Japan. The ideal candidate will have extensive experience in drug safety and clinical trials, with a focus on effective communication and organization.

Skills & Requirements

Must-have

  • Safety Management Plan authoring
  • SAE data review and entry
  • Regulatory reporting and submissions
  • Safety database management
  • Global regulatory guidelines knowledge

Nice-to-have

  • Bid defense presentations
  • Mentoring new staff
  • Pioneering and creative approaches

Key Requirements

  • Minimum of 5 years of pharmacovigilance experience
  • Bachelor’s degree in a science-related field, or nursing, or equivalent
  • Fluent in written and verbal English
  • Ability and willingness for potential limited travel

Work Rights

Not specified

Tailored Resume

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