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Kentucky Research Group will consistently:
- uphold the highest standards of ethical conduct and human subject protection as guided by the U.S. Food and Drug Administration, Code of Federal Regulations (Title 21, Food and Drugs) and ICH Guidelines for Good Clinical Practice.
- comply with standard operating procedures, protocal requirements, and applicable federal, state and local laws and regulations including, but not limited to, Health Insurance Portability and Accountability Act, Institutional Review Board, and Investigational New Drug regulations.
- deliver exceptional patient care.
- maintain timely, complete, accurate, organized, and verifiable regulatory documents and study-related clinical data.
- provide a comfortable, courteous and professional environment to accomodate the needs of our patients, research team and site visitors.
- ensure all clinical supplies, medications and documents are maintained in a secured, limited-access area, and study records are retained for the protocol-specified time period.
- utilize and maintain a patient database to assist with recruitment and contract enrollment.
- communicate and correspond appropriately with patients, research team members, and clinical trial contacts.
- establish, adapt and manage productive work schedules and priorities to achieve successful initiation and completion of all clinical research projects, tasks and assignments.
- identify methods and initiate efforts to increase/improve job knowledge and performance through additional research training, continuing education and certification(s).
- contribute positively and constructively to group goals to improve team performance.
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