pr jobs (salary & requirements)

Job summary:
We are seeking a senistudy director/project manager to manage ADME-PK projects with the working location at Shanghai (headquarters), Suzhou, Nanjing Qidong (Nantong) in China.
Role description:
Responsible fthe non-clinical ADME-PK studies integrated drug discovery to development programs.
Responsibilities:
1. Monitmanage non-clinical ADME-PK studies integrated drug discovery to development programs
2. Communicate proactively with clients propose ADME-PK study designs/program strategies to address key technical issues potential risks
3. Work as a study directon each study including but not limited to below list,
 Prepare high quality study protocol/design
 Lead the internal meeting fscientific discussion share study information clearly in time
 Oversee data collection, interpretation, analysis, documentation results reporting
 Deliver feedback report to clients in a timely manner maintain good relationship with existing clients
4. Work directly with all levels of management to address key technology information lead scientific discussion cross-functional teams/departments
5. Be able to consolidate in vitro/in vivo data, present in DMPK program review. Invite advices advocate scientific discussions as needed
6. Work with sales/marketing team on business development
Requirement:
1. Majored in Pharmacokinetics, Pharmaceutical Science, Analytical Science, Pharmacology, Medicinal Chemistry other related fields, Ph.D. is preferred
2. More than 5 years experiences in contract researchganization, academia, pharmaceutical industry is preferred
3. Fluent in both English Chinese (verbal written)
4. Excellent skills on communication