At Parexel, I processed and evaluated 3,000+ Individual Case Safety Reports from clinical studies, spontaneous reports, and post-marketing sources using Oracle Argus Safety and Artemis-IVP. I coded adverse events and medical history with MedDRA and followed SOPs and FDA/EMA guidelines.
I reviewed clinical trial data, medical histories, and statistical outcomes, and conducted quality checks to identify discrepancies and check compliance with SOPs and ICH guidelines. I also assisted with research, writing, and editing of scientific documents.
At RIMT University, I design and deliver lectures and practical lab sessions for pharmacy students, and evaluate assignments and papers. I mentor Diploma of Pharmacy students and assist senior faculty with coursework planning, academic administration, and assessment grading.
For my Master's thesis, I evaluated Byakangelicin in a vincristine-induced peripheral neuropathy model in Wistar rats. I conducted behavioral assessments and analyzed data from nociceptive assays and biochemical evaluations, including ELISA, SOD, and TBARS.
