SIRO Clinpharm is one of the leading Global Clinical Research Organizations (CROs), offering full scope services conducting clinical trials in the Pharmaceutical, Biotechnology and Medical Devices sectors in compliance with International Standards. We are headquartered in India having global presence in USA, Israel and in Europe at Germany, Czech Republic, Greece, Estonia, Romania, Spain and France.
Post: Documentation/Medical Writing
To assist the clinical project team in various in-house project related activities and maintain study documentation as per project instructions. This position is for 3 months on assignment basis.
In house support, communication in the project teams, filing, tracking and general administrative support. Prepare, maintain and update the in-house trial related files according to SOPs, Indian/ Applicable Regulations and ICH GCP.
Experience: 0-3 years
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: CR
End Date: 12th July, 2011
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