Trisha has over 30 years of experience in clinical research. She began her career as a CRA at Burroughs Wellcome Co (now GSK). She assumed increasing levels of responsibility, eventually becoming a Principal Clinical Research Scientist. During her time at GSK, she worked on studies in all phases of clinical development, including Phase 1. Since becoming a consultant, her primary work has been with regulatory writing and editing/QC for pharmaceutical and biopharmaceutical companies. Trisha’s therapeutic area experience includes psychiatry and neurology (depression, schizophrenia, restless legs syndrome, Parkinson’s disease, neuropathic pain, epilepsy, analgesia, and narcolepsy), respiratory (cystic fibrosis, smoking cessation, asthma, and chronic obstructive pulmonary disease), oncology, infectious diseases, anesthesiology, gastroenterology, gynecology, dermatology, nephrology, and vaccines. In the past 4 years, Trisha has authored documents that were components of 3 successful regulatory submissions.