I have worked in Clinical Research for 7 years with Covance and LabCorp now named Fortrea. I started out as a tech shortly after becoming a certified Medical Assistant. For the 2.5 years that I was a tech I performed blood and urine collections, obtained vital signs and ECGS, spirometry and other events to fill protocol needs. I became a Study Coordinator for 2 years where some of my responsibilities include reviewing protocols and I/E criteria, prepare and organize materials/procedures needed for study, and working with Investigators to ensure participant eligibility. Also, I assist with training staff on company SOPs as well as study specific trainings as needed. I have been a Project Coordinator for the past 2.5 years. I work closely with Project managers and other team leads in the start-up, maintenance, and close out of clinical studies. Working more independently my duties include creation of study specific documents, monitor training compliance, organize/schedule/attend study related meetings, and payment tracking to name a few. My strongest asset is my ability to be a team leader as well as be a team member. I demonstrate the ability to work in groups as well independently. Working with timelines i can produce quality work in an efficient and timely manner. Problem solving , proactiveness, verbal/written communication are additional assets I possess.