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Thursday, 13 February 2014

Drug Safety Associate / Senior Drug Safety Associate

Drug Safety Associate / Senior Drug Safety Associate 
ICON Clinical Research - Chennai, Tamil Nadu

Overview of the Role- 
  • Your primary responsibility will be validating and quality checking safety database fields on assigned projects. 
  • You will also provide input for and review relevant safety tracking systems for accuracy/quality and perform safety review of clinical data (case report forms) and patient labs. 
  • You will also be responsible for documenting and processing serious adverse event cases within ICON, regulatory authorities and sponsor regulations and timeframes. 

  • Role Requirements 
  • With a science degree, pharmacy or nursing background or equivalent, you will have previous experience in a drug safety environment together with strong knowledge of medical terminology. 
  • You will have knowledge of drug safety databases, preferably ARGUS. 
  • You will have the ability to produce high quality work, with meticulous attention to detail. 
  • You will be fluent in verbal and written English, with excellent communication skills. 

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