Associate, Non-clinical & Clinical Group

Sandoz

Head Office, Japan
Clinical monitoring
Clinical research
Document preparation for pmda
The role involves reviewing non-clinical and clinical data under the guidance of a manager

Job Summary

  • The role involves reviewing non-clinical and clinical data under the guidance of a manager.
  • You will participate in development strategy discussions and prepare submission dossiers.
  • The position requires interaction with PMDA during the review period to acquire necessary approvals.

Matching Summary

The role involves reviewing non-clinical and clinical data under the guidance of a manager.

Skills & Requirements

Must-have

  • Clinical Monitoring
  • Clinical Research
  • Document preparation for PMDA

Nice-to-have

  • Detail-Oriented
  • Negotiation Skills
  • Project Planning

Key Requirements

  • Experience in clinical trials
  • Knowledge of GCP regulations
  • Ability to prepare clinical study reports

Work Rights

Not specified

Tailored Resume

Cover Letter