DMPK Study Director

Key Accountabilities

  • To coordinate the entire process of pharmacokinetics (PK) studies from initiation of the study to the report writing for quality and timely delivery
  • To communicate with clients about technical details, project update and timeline
  • Scope of the Job
  • To design PK/PKPD/Tox studies, write study proposals, protocols, in-life summaries and study reports
  • To analyze, trouble shoot and interpret the PK data
  • To communicate internally with multiple groups (e.g. formulation, bioanalytical, in-life, non-GLP tox etc. for study arrangement)
  • To track project status, make sure all the studies completed on time.
  • To communicate with client for any issues occurred during project process. Work with the client to come up with solutions.
  • To work closely with Chemistry, Biology department, especially for integrate service project.
  • Provide weekly PK update to the project team.

Skills and Education

  • Ph.D. degree in biochemistry, biology, pharmacology or other related fields; Master’s degree with 3-4 years related work experiences.
  • Knowledge or hand-on animal handling experience is preferred.
  • Knowledge of basic principles of pharmacokinetics and data analysis
  • Familiar with and able to comply with IACUC, SOP, EHS regulations is a plus
  • Able to work well in a team
  • Good written and reading skills in English
  • Previous working experiences in CRO or pharmaceutical company are preferred.

Location: ZJ Hi-tech Park,Shanghai, China

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1F & 3F, Block A
2829 JinKe Road
Zhangjiang Hi-Tech Park
PuDong New Area
Shanghai China, 201203


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