Tokyo IQVIA Full time

Job Description

Key Responsibilities:

  • Facilitate post-manufacturing and sales investigations, ensuring facility compliance.
  • Provide investigation explanations and requests to medical institutions.
  • Handle contract procedures.
  • Collect and conduct re-investigations as necessary.
  • Manage the progress of investigations.
  • Complete final investigation procedures.

PMS Monitor Requirements are constantly evolving, with IQVIA prioritizing the development of PMS Monitors through additional GCP training menus.

Given Japan's position in the global Phase IV landscape, a strong capacity for GCP-like quality and Safety management is expected.

Training and Development Opportunities:

  • GCP Training (e-learning, Face-to-Face, CRA Certification Exam, Oncology Specialist CRA Certification)
  • CRA Accompanied OJT
  • Compliance Training (Introduction, Continuation)
  • Familiarity with Real-World Data Utilization and Environmental Trends

Requirements:

  • A minimum of 1 year of experience as a PMS Monitor or CRA.
  • At least 2 years of experience as a CRC, MR, or MS holder.
  • The ability to effectively utilize English in work-related activities (no prior English level requirements).
  • Oncology experience.
  • Experience working with university hospitals or core hospitals.
  • English communication skills (email, document creation, meetings).

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We aim to create a healthier world by pushing the boundaries of human science and data science.



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