Experienced Drug Safety Physician, Medical Monitor, Anatomic and Molecular Pathologist with strong expertise in pharmaceutical drug development industry performing medical review of AE/SAE/SUSAR ICSRs, aggregate reporting (DSUR, PSUR/PBRER & 6mLL), medical monitoring, signal detection/work-up, the interpretation of laboratory testing, diagnosis, and summary of complex medical safety data using TLFs. Good knowledge of CIOMS, EMEA GVP, GCP (Good Clinical Practice) and ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use) guidelines.