Currently employed with a leading clinical research investigator site, I have extensive experience in the healthcare and clinical research industry as well as project management. In my current role as Clinical Research Coordinator, I enjoy the responsibility of leading clinical studies and coordinating projects from conception to delivery based on the study protocol. During my tenure at Thomas J. Stephens & Associates, Inc., I began as an entry level Clinical Research Coordinator and was promoted to Quality Assurance / Reports Manager where I was responsible for creating and reviewing clinical study reports and case report forms, development and execution of training programs, and overseeing the corporate Quality Management System for a multi-site Contract Research Organization specializing in the field of clinical testing for cosmetics, personal care products, prescription, and OTC drugs.
I believe that my strong background in clinical research and process management, combined with my extensive experience in planning, executing, monitoring, and closing a variety of projects, makes me ideally suited for the Clinical Research Coordinator role. I am highly organized and self-motivated, have excellent communication skills, and thrive in high-pressure environments. I understand how to meet deadlines and actively facilitate the delivery of clinical research data.
I have a Bachelor of Science in Biochemistry as well as a Master’s in Health Administration. I have effectively implemented procedures in my previous roles for project scheduling, issue tracking, and resource management. I am also experienced in audit planning, scheduling, and execution.
My goal is to continue learning and developing my expertise in clinical research and healthcare. I began my career as a Clinical Research Coordinator and I believe I enjoyed my job the most in this role.