1. Monitor and manage non-clinical ADME-PK studies and integrated drug discovery to development programs
2. Communicate proactively with clients and propose ADME-PK study designs/program strategies to address key technical issues or potential risks
3. Work as a study director on each study including but not limited to below list,
Prepare high quality study protocol/design
Lead the internal meeting for scientific discussion and share study information clearly and in time
Oversee data collection, interpretation, analysis, documentation and results reporting
Deliver feedback and report to clients in a timely manner and maintain good relationship with existing clients
4. Work directly with all levels of management to address key technology information or lead scientific discussion cross-functional teams/departments
5. Be able to consolidate in vitro/in vivo data, and present in DMPK program review. Invite advices and advocate scientific discussions as needed
6. Work with sales/marketing team on business development
任职要求
1. Majored in Pharmacokinetics, Pharmaceutical Science, Analytical Science, Pharmacology, Medicinal Chemistry or other related fields, Ph.D. is preferred
2. More than 5 years experiences in contract research organization, academia, or pharmaceutical industry is preferred
3. Fluent in both English and Chinese (verbal and written)
4. Excellent skills on communication
