Master of Science in Clinical Research Organization and Management

36.0 semester credits


The Master of Science in Clinical Research Organization and Management consists of 12 courses. Any courses offered by the Clinical Research Organization Management program may be applied to fulfill the requirements of this major.

The program is organized into five areas of study devoted to clinical research and related administrative and regulatory issues. Students can take courses within their preferred area of study, a cross-section of courses within other areas of study, or any other CR courses being offered.

Areas of study:  
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
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
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
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
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