【COMPANY OVERVIEW】
Global Biotechnology company focusing on innovative precision based cancer therapies
【JOB RESPONSIBILITIES】
Contribute to the development the strategy from nonclinical perspective.
Provide / lead the nonclinical-related parts of regulatory documents.
Interpret the outcomes from studies for clinical and plan/manage appropriate studies.
【WHY YOU SHOULD APPLY】
You will be the pioneering person for this role in the company
Career development support (training and promotions)
Start up company environment with strong financial backing and rapidly expanding.
Working with a diverse and motivated team with excellent work culture.
【REQUIREMENTS】
10 + years Knowledge of relevant role with oncology products.
Comprehensive knowledge/skills of either the field of pharmacodynamics, pharmacokinetics and/or toxicology.
Current knowledge of molecular biology and ICH guidelines / Japanese guidelines for nonclinical studies of drugs.
Knowledge of new drug development process and procedure.
Very good communication and problem solution skill among cross-functional team.
Ability to communicate reading, writing and speaking in English (Target TOEIC 800 + )
Bachelor's Degree in science or related discipline