I have 25 years of experience in the research industry with approximately 12 years in the CRA role, a few years as a Study Coordinator/Data Manager/Research Nurse, Product Safety Associate, Coder, and one and a half years as an IRB Coordinator with some roles crossing over. Responsibilities included preparing and submitting protocols to the IRB, collaborating directly with subjects, monitoring the progress of clinical trials at investigative sites, ensuring subject safety, data integrity, ensuring trials were conducted according to protocol requirements, as well as ensuring SOPs, ICH/GCP, and all applicable local, and regulatory requirements were followed. Throughout my career, I have worked in a variety of therapeutic areas including oncology and trials ranging from phase I-IV and post-registry trials in both industry as well as Cooperative Group studies. I also played a significant role as a team lead and assisted with monitoring visit sign offs for junior level CRAs. In addition, I mentored, instructed, and took the initiative to teach others.