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ChatSenior Role - Drug Safety #lifesciencegraduate #nagpurjobs #apportunities #clinicalresearchinstitute #smo #clinicalresearchcareers #clinicalresearchtrials #medicalresearch #healthcare #biology #pharmacovigilance #clinicalresearchtraining #education #bpharma #research #clinicalresearchers #nurse #clinicalresearchjobs #crc #pharmaceuticals #pharma #clinicaltrialsguru #clinicaldatamanagement #cralife #sciences #pharmacy #training #careers #rn #clinicaltrialsday pharma job alert 1.Reviewing the published reports/biomedical literature to ascertain if they contain individual case reports and Non-individual case reports. 2. Applying regulatory and internal guidance to determine if the article meets the definition of a valid case report and Non- individual case reports. pharma job alert 3. Write accurate and concise summaries that capture the key elements from these published reports 4. Ensure consistent coding of medical history, drugs and adverse event terms pharma job alert 5. Evaluation of Serious Adverse Event to ensure accurate processing from source documents with emphasis on quality and timeliness pharma job alert 6. Creating summary content in a range of formats (narrative summaries, structured database inputs, electronic formats for regulatory filing) to support the drug safety reporting and information requirements of pharma industry client M.Pharm / B.Pharma / BAMS / BHMS / PhD./ Pharm D / BDS
Senior Role - Drug Safety
Micro Labs Limited emerges as a preeminent technology-driven healthcare entity, recognized for its cutting-edge Research and Development (R&D) and state-of-the-art automation-driven manufacturing facilities. The company consistently excels in international regulatory audits, reinforcing its commitme...