April D

Clinical Research - 6 Years of Experience - Near 80918


Clinical Research

Education Level:


Will Relocate:



Pursuing a challenging career in an organization where I can apply my talents and education in a medical/scientific-related field. Qualification Highlights Proficient use of Databases: iMedidata RAVE, RTOG, GOG, Inform, Oncore, CTSU, SWOG, Clincapture. Oversee RNs are strictly following X-Chart requirements of study protocols. Reviews Expectancy Reports of all associates in our department to ensure data timelines are met. Responsible for timely patient data management and submission. Screens daily Gyn/Oncology doctor's schedules and pathology reports for potential study participants. Revised and updated department's Standard Operating Procedures. Provides guidance to the research nurses that study specific protocol requirements are met. Prepares study specimens for collection, observing protocol required processing and shipping instructions following Category B Biological Substances regulations. Certified in ICH GCP Principles and the Code of Federal Regulations (CFR). Screened patients and consented for The Cancer Genome Atlas Study. Prepares on a daily basis patient charts for their study appointments ensuring all current medical records are printed and any study specific requirements including QOLS and specimens. Assisted the cardiology research nurses with screening of patients for studies using Nexgen system. Proficient in computer applications, to include Mosaic, Meditech and Microsoft Office. Avid learner with an ability to rapidly achieve organizational integration, assimilate job requirements and employ new ideas, concepts, methods and technologies. An energetic, innovative and self-motivated team player.