About the job

• Reviewing the published reports/biomedical literature to ascertain if they contain a case report of an adverse reaction and Non- individual case reports.
• Applying regulatory and internal guidance to determine if the article meets the definition of a case report and Non- individual case reports.
• Perform relevancy assessment based on accepted industry guidelines.
• Provide training and guidance to the scanners on inclusion criteria of case report and Non- individual case reports.
• Work closely with the SMEs to ensure physician team has necessary training and skills per industry norms.
• Perform additional tasks/responsibilities as assigned delegated by the team lead/manager
  

Qualifications

MD / MBBS,M.Pharm / B.Pharma / BAMS / BHMS / PhD./ Pharm D / BDS

Apply through below link

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