Support establishment of clinical development strategies for the investigation of new drugs
Review information about early clinical trials including initial clinical dose setting and pharmacokinetic interpretation and analysis, consulting, drug interaction prediction, academic support, etc
Post-marketing drug surveillance
Medical Writer : arranging post- marketing PV documents to maintain drug licensing
Signal detection : review and risk assessment of drug safety information periodically analyzed
Case Processing : Argus
Database Entry, Medical Review
Education : graduated from medical faculty Indonesia (S.Ked)
Language : fluent in English
Having knowledge about clinical test and experience iresearch
Having medical knowledge, sufficient understanding of drug surveillance and able to review the related safety standard
Able to review documents and prepare papers to be submitted to regulatory agency
High understanding about IPF treatment and able to give medical advice
Able to provide medical advice on autoimmune diseases, gastroenterology, oncology, neurology, etc.
Having high understanding of clinical-related medicine such as pharmacology, pharmacokinetics, and clinical statistics