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Job Description

Company Overview
Global Pharmaceutical Maker

Job Description
• Responsible for non-clinical safety evaluations of multiple complex projects with in-depth knowledge of toxicologic pathology in accordance with all applicable guidelines/regulations in close cooperation with other BI sites
• Leading interactions with Japanese regulatory agency
• Contributing to global safety-related activities within BI

Requirements
• Doctoral Degree (PhD or MD博士修了) with a minimum of 5 years’ experience within pharmaceutical R&D
• Proven performance record in the field of responsibility (ideally >3 drug development projects)
• Board certificate in Toxicologic Pathology / Veterinary Pathology (JSTP, JCVP or equivalent) or Board certificate in Toxicology (JSOT or equivalent)
• Exceptional level of knowledge in the field of responsibility (Toxicology/Pathology)
• Knowledge of GLP and regulatory compliance
• Good connection with academia and authorities