[phpWebLog-devel] first name cough

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The candidate will also perform blood processing experiments using
microfluidic systems and analyze data. 
Responsible for planning, designing and executing clinical protocols
supporting a specific therapeutic such as Oncology, Cardiology,
Rheumatology or Neurology. 
Ability to read a lot of material and condense the information.
Knowledge of carrying out, prior art search using databases and
Infringement analysis. To work in accordance to GLP. Responsible for
supporting pre-clinical and clinical development of HCV compounds. 
D in pharmaceutical sciences. 
The candidate will also perform blood processing experiments using
microfluidic systems and analyze data. 
Formulation development for cytotoxics - including intravenous
formulations. 
Interact with bug tracking system to monitor fixes and retests. 
Ability to read a lot of material and condense the information. Good
communication skills. After the constructs are clone into the suitable
vectors they are mobilised into the Agrobacterium Strain. For each
position, I have listed a short description and a link for more
information. 
Exposure in patent law of USA, EP etc. 
Candidates well versed with GLP, FDA and other regulatory requirements
will be preferred. Provide pharmacovigilance input on designated
products, including signal detection and monitoring, formulation and
preparation of ad hoc regulatory responses. 
To produce and manage material for a variety of scientific disciplines.
Manages clinical staff and clinical projects, including CROs and
contract labs. 
Board certified or board eligible is preferred. After the constructs are
clone into the suitable vectors they are mobilised into the
Agrobacterium Strain. This position will be responsible for production
of analysis datasets and specifications, well documented code, summary
tables and some statistical analysis of data. 
Those who have interest in doing quality projects and expand their
carrier growth are welcome. 
Review AE data, PSUR reports and PMS reports. The candidate will perform
data entry, data clean up, and data loading to maintain and expand a
commercially successful database of available chemicals. 
Good communication skills. Review AE data, PSUR reports and PMS
reports. 
Make recommendations to Corporate Drug Safety Committee, as
required. 
Monitoring of Adverse Events from clinical trials. 
Interact with pharmacovigilance units in countries. 
Provide pharmacovigilance input on designated products, including signal
detection and monitoring, formulation and preparation of ad hoc
regulatory responses. 
Experience in sterile cell culture procedures, cell processing is
needed. 
To work in accordance to GLP. 
Effectively leads a global team of individuals assigned to the
protocol. 
 
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