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Master of Science in Clinical Research Organization and Management
36.0 credits.

The Master of Science in Clinical Research Organization and Management consists of 12 courses. The program combines five areas of study devoted to clinical research and related administrative and regulatory issues. Students take courses within their preferred area of study, as well as a cross-section of courses within the other areas of study.

Curriculum
Track #1 New Product Research and Development
CR 513S	Pharmaceutical R & D Business Process and Information Flow		3.0
CR 514S	World Wide Regulatory Submissions		3.0
CR 515S	Introduction to Clinical Trials		3.0
CR 609S	Innovative Product Development		3.0
CR 620S	Biotechnology: Principles, Practices and Regulations		3.0
CR 620S	Biotechnology: Principles, Practices and Regulations		3.0
Track #2 Regulatory Compliance, Ethics and Law
CR 505S	Ethical Issues for Clinical Research		3.0
CR 511S	History of Misconduct in Biomedical Research		3.0
CR 535S	Current Federal Regulatory Issues in Biomedical Research		3.0
CR 555S	Issues in Compliance and Monitoring		3.0
CR 565S	Contemporary Issues in Human Research Protection		3.0
CR 633S	Quality Assurance Audits		3.0
CR 612S	Fundamentals of Compliance		3.0
CR 545S	Pharmaceutical Law		3.0
Track #3 Biostatistics and Data Management
CR 500S	Epidemiological Methods for Clinical Research		3.0
CR 520S	Applications of Clinical Research Biostatistics		3.0
CR 560S	Special Topics		3.0
CR 600S	Designing the Clinical Trial		3.0
Track #4 Clinical Research Management and Safety Surveillance
CR 512S	Fundamentals of Academic Research Administration		3.0
CR 525S	Scientific Writing and the Interpretation of Medical Literature		3.0
CR 625S	Health Policy and Pharmacoeconomics		3.0
Track #5 New Therapeutic Product Business and Strategic Planning
CR 530S	Technology Transfer and Intellectual Property		3.0
CR 635S	Strategic Planning		3.0
CR 550S	Leadership Skills		3.0