Requirement of Data Reviewer / Medical Writing @ SIRO Clinpharm
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: Data Reviewer/Medical Writing
To perform the data management activities for the assigned studies as per the scope of the job role and task assigned. 1. CRF Designing 2. Database designing 3. Edit Check Programming 4. Data Validation 5. Drafting of CDM SOPs as assigned.
One year experience in the Clinical Data Management Department as Data Reviewer. B.Sc, B.Pharm, M.Pharm & M.Sc candidate
Experience: 1-5 years
Education: B.Pharm, M.Pharm, B.Sc, M.Sc
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: CR
End Date: 20th July, 2011
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