Kenneth Quick Email and Phone Number

• Knowledgeable in 'Good Clinical Practices', federal, state and regulatory for clinical research and Institution Review Board guidelines.• Experienced in the informed consent process, and ability to properly conduct informed consent when enrolling patients into studies.• Proficient in computer skills such as MS Word, MS Excel, and MS Outlook, as well as patient and research databases.• Excellent communication skills to work effectively with research subjects, physicians, hospital and clinical personnel, research sponsors and representatives.• Exceptional interpersonal skills demonstrating professionalism, compassion, and resourcefulness when interacting with a diverse population of patients.• Organizational skills to manage multiple clinical studies, coordinate multiple tasks and to appropriately prioritize workload • Skillful in Management of multiple clinical trials and research studies, including recruitment, screening, enrollment, informed consent, data collection and management, study audits and monitoring visits, study closeouts, lab specimen processing, and sponsor communications