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: Clinical Researcher
This position will be responsible for management of standard operating procedures (SOPs), management of audit and inspection files, to conduct audits and to perform a quality assurance review of clinical study documents.
Standard operating procedures (SOPs), manage audit files and inspection files, as designated perform QA, review of clinical study documents, conduct audits, clinical trial supplies and services oversight compliance support. Pharmacy candidates only.
Experience: 2-5 years
Education: B.Pharm, M.Pharm
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: CR, QA
End Date: 29th May, 2011
THIS JOB IS EXPIRED !
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