- Manage and report on all in vitro and in vivo nonclinical toxicology IND enabling studies and studies supporting more advanced clinical stages
- Work closely with internal functional groups such as Pharmacology, ADME-PK, CMC, Regulatory Affairs, Clinical Development, and Program Management, and actively participate in team strategy discussions for drug development programs
Manage Non-Clinical Safety Group at a Leading European Pharma Maker
Contribute to Overall R&D Mission to Gain Approval for Life Changing Medicines
Our client is looking for an individual that is motivated to lead the business innovation and support the digital experience of the end users in Kansai, Japan.
Lead business strategies with Big Data and multi-channel management
Good work-life balance and international work environment (in KANSAI)