Clinical Research Administration Eastern Michigan University

Overview

The Clinical Research Administration M.S. at Eastern Michigan University is designed to provide students with the advanced knowledge and practical skills required to excel in the rapidly expanding field of clinical trial management. This programme addresses the growing demand for qualified professionals capable of coordinating complex research studies and navigating global regulatory frameworks. Students benefit from a curriculum that blends theoretical foundations with real-world applications in the pharmaceutical and biotechnology industries.

Why Clinical Research Administration at Eastern Michigan University?

Eastern Michigan University was a pioneer in establishing academic credentials for this field and remains a recognised national leader in clinical research education. The programme is distinguished by its strong industry links and collaborative partnerships with prestigious organisations such as the Henry Ford Health System, AstraZeneca, and the University of Michigan Hospital. These connections provide students with unique insights into the clinical research enterprise and enhance their professional networking opportunities.

The curriculum is delivered through a hybrid format, combining face-to-face instruction with online learning to accommodate working professionals. As a designated STEM programme, it focuses on the rigorous scientific and regulatory standards necessary for the development of new drugs, biologics, and medical devices. Students also have the opportunity to engage in optional hands-on preceptorships, gaining direct experience in clinical study environments.

Tuition Fee Breakdown

• International fee: USD 20916 per year
• National fee: USD 20916 per year
• Local fee: USD 12068 per year

Visit the Fees and Funding section for a breakdown in your local currency.

Syllabus

The curriculum consists of 34-35 credit hours, focusing on the lifecycle of drug development and the ethical management of human subject research. Modules may include:

• Drug Development
• Clinical Study Administration
• Advanced Topics in Clinical Study Management
• Ethical Issues in Clinical Research
• Regulatory Affairs in Drug Development
• Graduate Seminar in Drug Development
• Regulation of Medical Devices
• Regulatory Writing and Electronic Submissions
• Epidemiology

Careers with Clinical Research Administration

Graduates are prepared for diverse leadership roles within the pharmaceutical, biotechnology, and medical device sectors. The programme provides a clear pathway for upward mobility, enabling professionals to transition into senior management positions or specialised regulatory roles. Common career paths include clinical trial coordination, study monitoring, and data management, where graduates interface directly with global regulatory agencies to ensure compliance and safety in medical research.

The expertise gained at Eastern Michigan University allows alumni to contribute to the development of vaccines and life-saving therapies. By mastering Good Clinical Practice (GCP) and federal regulations, graduates become essential assets to contract research organisations, academic medical centres, and private industry partners involved in the clinical research enterprise.