Eastern Michigan University's Clinical Research Administration MS Program is a two-year graduate course designed to equip students with the necessary knowledge, skills, attitudes, and abilities to succeed in the clinical research field. The program responds to the rapid growth in pharmaceutical, biotechnology, and medical device research, as well as increased collaborative efforts between industry and academia. It aims to produce a qualified workforce capable of coordinating and monitoring clinical trials and managing data interfacing with global regulatory agencies. The program combines didactic coursework with optional hands-on preceptorships, offering a comprehensive educational experience. Courses cover drug and device development, Good Clinical Practice, regulatory affairs, clinical protocols, research ethics, study management, and more. Offered in a hybrid format, it is accessible to non-traditional students balancing full-time employment.
Why this course is highly recommended
This program is a leader in its field, developed as one of the first academic programs credentialed for clinical research administration. It is supported by major healthcare and research organizations such as Henry Ford Health System, Karmanos Cancer Center, and the University of Michigan Hospital, among others. Its curriculum is designed to meet the expanding demand for well-qualified clinical research professionals, ensuring graduates are prepared for upward mobility and diverse career opportunities within the expanding clinical research workforce.
The program specializes in clinical research administration, focusing on drug, biologic, vaccine, and medical device development processes. It emphasizes understanding federal and international regulations, clinical study management, ethics, and research project development. With electives available in areas like epidemiology, regulatory affairs, healthcare management, and law, students can tailor their study to align with specific career interests while gaining a broad understanding of clinical research operations.
Application fees
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1st year tuition fees
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Living cost
To earn the MS in Clinical Research Administration, students must complete 34-35 credits, including required coursework, electives, and a thesis or project option. The core courses encompass drug development, clinical study administration, research ethics, and regulatory affairs. Electives allow students to deepen knowledge in related fields, and the program encourages research or practical projects as part of the graduation process. The coursework must be completed within six years of enrollment, with specific residency and GPA requirements to ensure academic progress.

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Graduates of this program will be prepared for roles in clinical research coordination, management, and regulatory affairs within pharmaceutical, biotechnology, and healthcare organizations. The program aims to provide qualified personnel to support the clinical research enterprise, which is experiencing significant growth. It also provides opportunities for current professionals to advance their careers in clinical trial management, regulatory compliance, and industry leadership.