A medical professional with comprehensive knowledge of drug development process, regulations/guidelines and global drug safety and have 3+ years of experience in pharmacovigilance and medical writing across a wide range of products and multiple therapeutic areas including oncology, immunology, neurology, endocrinology, reproductive, etc. I have a graduate degree dental surgery and a post-graduate diploma in Clinical Research and Pharmacovigilance. Experience in end-to-end authoring and editing of clinical and regulatory documents, patient and HCP information brochures and slide decks. Ability to interpret and present complex clinical data and other information in a medically-relevant manner. In-depth knowledge of regulatory submission criteria, regulatory timeline requirements, FDA, ICH, Medicines Australia and TGA guidelines and medical terminologies. Strong communicator with excellent English grammar, writing and editorial skills.