Clinical Safety Coordinator

Japan Permanent Foreign Multinational
  • Develop Innovative New Drugs at a Leading Global Contract Research Organization
  • Contribute the Safety and Wellness of Patients Globally

About Our Client

  • Expanding US based CRO focused with growing presence in Asia

Job Description

  • Working closely with the Clinical Safety Manager to ensure each project deliverables are met
  • Collect, process, and track serious adverse event (SAE) reports and clinical event documents;
  • Generate and track study report safety narratives;
  • Coordinate safety surveillance activities (e.g., lab review and trend analysis);
  • Generate Investigator Safety Letters and distribution to health authority;
  • Assist in preparation of clinical safety documents

The Successful Applicant

  • Hands-on experience in pharmacovigilance case processing (data entry, triage, evaluation, QC, submission).

  • Japanese language proficiency of business level

  • Ability to prioritize, time line management

  • Ability to read and write short sentences using English dictionaries

  • Bachelor's degree or higher

What's on Offer

  • Opportunity to build leadership skills and move into a management position
  • Opportunity to work on a large number of diverse projects to develop a broad range of IMPs
  • Work on global studies at an industry leading international company
Ed Marsden
Quote job ref
Phone number
+813 6832 8981

Job summary

Job Type
Consultant name
Ed Marsden
Consultant phone
+813 6832 8981
Job Reference
Company Type