New York, New York, United States
My years of experience within the healthcare sector have furthered my understanding of patient burden and the need for comprehensive medical solutions. The intersection of research, biotechnology, and pharmaceuticals offers insight into the constant improvement in both quality of life and in how we approach medicine as whole. The future of medicine is advancing at lightening speed which requires an adaptable and dynamic individual as myself to bring understanding and discernment to it. My goal with every professional position I hold is to advance both personal and interpersonal achievements, while making a lasting and meaningful impact through my work.
-Conduct site qualification, initiation, monitoring, and close-out visits according to ICH-GCP, Medpace/Sponsor SOPs, and applicable regulatory requirements -Responsible for overall site management for assigned sites, including written and verbal communication and scheduling of monitoring visits -Responsible for completion of visit reports, follow-up letters, and maintenance of study-related databases -May serve as Lead CRA on a project, acting as the primary contact for monitoring-related questions and Monitoring Plan development/maintenance -Act as resource and facilitate training for new CRAs -CRA mentor and trainer -Clinical indications experience: Genetic Diseases, Infectious Diseases, Hypertriglyceridemia, Cardiovascular, Lipidemia ]
-Performed and assisted with medical and technical procedures within a team setting, according to plans of care -Facilitated open communication between various healthcare workers and patient needs -Documented and recorded patient health and diagnostic data