The Clinical Research Coordinator acts as the clinical research coordinator for projects in the Department of Urology. The primary responsibilities of the position involve day-to-day management of clinical trials in areas of data management, regulatory administration and direct patient contact relating to new and ongoing clinical research in the department. These trials can be both industry-sponsored and investigator-initiated studies. Coordinates and follows through in the overall administration and outcome of clinical studies.
Demonstrated knowledge of Federal, State and local regulations for conducting research on human subjects
Knowledge and understanding of basic anatomy and medical terminology; knowledge and understanding of urology and disease processes as applied to clinical research highly preferred
Demonstrated experience completing regulatory documents (FDA1572, Financial Disclosure Forms) and other required study start-up procedures
Familiarity with IRB administration and document preparation
Working knowledge of study budget preparation; ability to perform basic accounting processes
Displayed organizational skills and attention to detail so that large volumes of records can be accurately maintained
Experience composing correspondence and writing reports
Analytical skills to independently and tactfully assume responsibility for coordination and completion of complex projects requiring interactions with many individuals in a matrix organizational structure
Experience working with Microsoft Office, Excel, Outlook, Epic EMR and various industry Electronic Data Capture Systems
Certification by Society of Clinical Research Associates and/or Association of Clinical Research Professionals highly preferred.
Bachelor's degree in related field
THIS POSITION MAY BE SUBJECT TO A CRIMINAL BACKGROUND INVESTIGATION, DRUG SCREEN, LIVE SCAN FINGERPRINTING, MEDICAL EVALUATION CLEARANCE, AND FUNCTIONAL CAPACITY ASSESSMENT
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