Clinical Research Coordinator
July 2016 — Present
• Responsible for the implimentation and coordination of clinical trials by accurately performing the informed consent process, obtaining patients’ medical history and concomittant medications and procedures, performing study procedures per protocol, and maximizing sufficient documentaition in source documents and electronic data capturing.
• Performed electrocardiograms, venipuncture and specimen processing and shipping, blood pressure, height, weight, and temperature measurements.
• Well versed in reporting adverse events and working with prinicpal investigators.
• Managed Five Clinical Trials ranging from Migraines, Hypertriglyceremia, Type II Diabetes Meillitus, Cardiovascular Disease, and Osteoarthritis.