In this role, the selected candidate will ensure that the consent process has taken place effectively and all questions are answered satisfactorily and documented; process and prepare specimens for lab analysis and shipping.
In this role, the selected candidate will assist manager in the efficient operation of unit including fiscal and human resources; participate as a team member by performing additional assignments not directly related to the job description when workload requires.
CRNC is responsible for coordinating the research activities of IRB-approved study protocols. Specific protocols that require the CRNCs support will be determined by the Department Head of Clinical Investigation Department (CID) in consultation with the Clinical Research Coordinator.
In this role, the selected candidate will utilize knowledge of the principles of growth and development over the life span of patients and demonstrates knowledge and clinical skills necessary to provide care appropriate to the age and population of the patients served.
In this role, you will be responsible for coordinating the research activities of assigned IRB-approved study protocols Reports and is responsible to the Principal Investigator (PI) and supports the CID department head in accordance with federal and local regulatory guidelines.
In this role, you will be responsible to performs research; analysis; development and evaluation of systems; procedures and models in assigned functional area. Analyzes and defines problems and researches possible solutions that afford maximum probability for profit or effectiveness in relation to cost or risk.