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DMPK Study Director

The Programme 

公司在全球设立了6个办事处,专职研发人员2000人,海归科学家150人,拥有大规模最先进的科研、办公设施、实验动物设施、cGMP级别的公斤级实验室以及医药中间体生产设施。公司通过坐落于张江、奉贤、启东、成都和南旧金山五个重要研发基地持续不断为来自全球范围内客户长期提供优质的服务。 

Responsibilities 

  • 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, bianalytical, 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.  

Required Skills and Abilities 

  • Bachelor degree in biochemistry, biology, pharmacology or other related fields. 
  • 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. 
     
     
     
Closing in 4 days
Closing in 4 days
  • Job type:Graduate Jobs
  • Disciplines:

    Pharmacy and Pharmacology

  • Citizenships:

  • Locations:

    Shanghai

  • Closing Date:31st Jul 2021, 6:00 pm

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