Skilled at collecting specimens, dispensing medications and consulting with patients during the course of clinical research trials. Experienced in coordinating schedules, results and documentation. Knowledgeable CRA adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues.
Assists with the implementation and conduct of clinical research projects as delegated to assure successful achievement of quality, safety, regulatory and financial outcomes including maintaining regulator binders, recruiting and retaining study subjects, research billing compliance, performing procedures, collecting data and query resolution.
Performs specific technical tasks and procedures that may include performing phlebotomies, recording test subject's vital signs, height and weight, collection and distributing diaries and questionnaire and other study specific procedures or test as assigned. Record data.
Maintains inventory of study-specific supplies and clinical supplies. Works to assure protocol compliance and efficient workflow including, organizing clinical work areas, counting and ordering kits and shipping materials, and checking and replace expired items.
Assist the research team in the implementation of conduction research studies. Performing task delegated to me in a timely I schedule appointments for our patient. Printed and Log all IND safety reports.
I assist with the Pedi Oncology Dept and collecting specimen and shipping.
Study protocols
undefinedI love to spend time with my wonderful husband, son, daughter-n-law and grandsons. When I'm home I like to work outside in the yard. Love to horseback ride, camping an going to church