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the Enterprise Resource Planning (ERP) systems. To enhance and maintain the system by analyzing, designing, estimating, developing, documenting, testing and implementing required changes. To act as a direct
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Information Technology Security Policies and participating in security training, such as Health Insurance Portability & Accountability Act (HIPAA) and Family Education Rights and Privacy Act (FERPA), on an annual basis
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associated personnel. To design best practices for management of IP for drug, device, and biologic studies. To prepare study budgets. To manage research staff within area including all applicable human
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protocols and the associated personnel. To serve as a resource person or act as a subject matter expert (SME) within area of clinical expertise. Key Duties & Responsibilities Management of multiple memory
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, and collecting various assessments such as adverse event (AE) information or questionnaires. To perform the informed consent process following GCP. To act as a liaison among the clinical and research
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a systematic critical-thinking approach to guide data gathering, assessment, nursing judgment, intervention and evaluation of human responses to actual and potential health problems through activities