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: Sr Medical Writer/Medical Writer
Develop Clinical Study Reports, Narratives, Protocols, ICFs, IBs, Safety Reports, Efficacy Reports and other regulatory submission documents as per ICH guidelines
Create CSR / ASR shell. Prepare appendices
Interpret statistical tables scientifically
Dr. (MBBS, BHMS, BAMS), MD, Ph.D. or Post graduate in Pharmacy or life sciences with at least 2 years experience in MW.
Awareness of GCP and regulatory guidelines related to Safety Reporting
Good English Communication and Analytical Skills
Experience: 1-5 years
Education: MBBS, M.Pharm, Ph.D, MD
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: CR
End Date: 24th Dec, 2011
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