As a regulatory affairs or clinical research professional, you will lead and play a significant role in the development and advancement of medical products for some of the biggest companies and agencies in the country. You will engage in the design, manufacturing, and testing of products to make sure they comply with the regulations and standards of the industry. The MS in Regulatory and Clinical Research Management (RCRM) allows you to start or advance a career in the increasingly complex and growing areas of commercialization of drugs, medical device products, biologics, regulatory affairs, and clinical trial operations, compliance, and management.
Regis offers dedicated assistance with both internship and job placement. Every student in the program receives real-world experience allowing you to apply classroom learning in a professional setting to develop skills, learn from professionals in the field, and build your professional network.