• Leadership in the design and development of a multi-disciplinary research and Clinical Trial program
• Support Director, research fellows, and other team members in their roles in developing this program (Task scheduling, enrollment oversight, and standard operating procedures)
• Prepare research documents, presentations manuscripts, grant proposals, and journal articles pertaining to the basic science and clinical research focus of the group;
• Manage research activities, including oversight of coordinating research protocols
• Assist research administration in grant submissions and philanthropic program needs
• Maintain effective communication and integration with national and international "partner" institutions;
• Develop novel procedures and other linkages for the program;
• Perform Needs Assessments and Program Evaluations, involving extramural consultants as required such as regulatory audits
• Develop and maintain program web site, incorporating active programs and research;
• Organize occasional conferences and related activities (e.g., strategic planning workshop);
• Support growth of program: developing procedures, streamline operational tasks, and increase efficiency and optimal work load for growing program
• Other duties as assigned

Bachelor's degree in science-related field and 5+ years of related experience required. Extensive understanding of regulatory coordination of protocols oversight and IRB guidelines and process for managing robust clinical research program.

PI288085295