[phpWebLog-devel] first name cough
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From: Isaac F. <sq...@od...> - 2006-10-20 12:51:41
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<!DOCTYPE html PUBLIC "-//W3C//DTD HTML 4.01 Transitional//EN"> <html> <head> <meta content="text/html;charset=ISO-8859-1" http-equiv="Content-Type"> </head> <body bgcolor="#ffffff" text="#000000"> <img alt="" src="cid:par...@od..." height="392" width="624"><br> The candidate will also perform blood processing experiments using microfluidic systems and analyze data.<br> Responsible for planning, designing and executing clinical protocols supporting a specific therapeutic such as Oncology, Cardiology, Rheumatology or Neurology.<br> 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.<br> D in pharmaceutical sciences.<br> The candidate will also perform blood processing experiments using microfluidic systems and analyze data.<br> Formulation development for cytotoxics - including intravenous formulations.<br> Interact with bug tracking system to monitor fixes and retests.<br> 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.<br> Exposure in patent law of USA, EP etc.<br> 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.<br> To produce and manage material for a variety of scientific disciplines. Manages clinical staff and clinical projects, including CROs and contract labs.<br> 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.<br> Those who have interest in doing quality projects and expand their carrier growth are welcome.<br> 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.<br> Good communication skills. Review AE data, PSUR reports and PMS reports.<br> Make recommendations to Corporate Drug Safety Committee, as required.<br> Monitoring of Adverse Events from clinical trials.<br> Interact with pharmacovigilance units in countries.<br> Provide pharmacovigilance input on designated products, including signal detection and monitoring, formulation and preparation of ad hoc regulatory responses.<br> Experience in sterile cell culture procedures, cell processing is needed.<br> To work in accordance to GLP.<br> Effectively leads a global team of individuals assigned to the protocol.<br> <br> </body> </html> |