Clinical Monitor - Global Med Device

Tokyo 23 Wards Permanent Foreign Multinational
  • Work from Anywhere in Japan
  • Work in a Leading Multinational Medical Device Area

About Our Client

  • Leading multinational medical device company
  • Rich product portfolio across several key therapeutic areas

Job Description

  • Develop and maintain relationships with investigative sites and client personnel
  • Monitor sites for accuracy and validity of entries related to patient records and clinical notes
  • Provide and communicate trial status and progress reports to trial manager and client
  • Manage and maintain the data and documents required by local and ICH regulatory authorities
  • Ensure SOPs are being followed and assist with client audits and regulatory inspections

The Successful Applicant

  • Monitoring experience in leading medical device company
  • Familiar with GXP, particularly GCP
  • English communication skills
  • bachelors degree (nursing, medical or life science related)

What's on Offer

Possible career progression opportunities as a CRA include:

  • Clinical operations line management
  • Clinical project management
  • Safety
  • Regulatory affairs
  • Clinical Data Management
  • Quality assurance / auditing
  • Site management and contracting

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