Responsibilities

• Maintains consistency with Administrative and Departmental policies with appropriate behavior, dress, attitude, attendance, confidentiality, professionalism, and reliability.
• Responsible for regulatory management of research protocols
• Assist the Primary Investigator in maintaining compliance with study and protocol specific guidelines
• Maintain and continually refine customized, networked computerized database to allow for timely tracking of research projects scheduled for re-review.
• Facilitate and maintain Institutional Review Board protocol submissions
• Screen and enroll patients into new protocols
• Contact, document and follow-up study participants to ensure study compliance
• Maintain timely submissions of regulatory and study documents
• Investigate new/potential research studies for various departments
• Track and report research information of grant funded studies

Requirements

• Bachelor's Degree in Healthcare Administration, Research, Business or related field preferred.
• Proficiency in using personal computer databases, spreadsheets and word processing software is required.
• Requires excellent oral and written communication skills.
• Requires excellent organizational skills and knowledge of federal legislation regarding human subject research and the provision of health care is also required.
• Expertise in applying for research protocols is required.
• Some travel to regional hospitals may be required.
• Proficient in organizing and examining data.
• Must be able to produce clear and concise products.
• Must be thorough in gathering and reporting information.
• Must be flexible and be able to relate well with a variety of people.