Program Overview

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.

Top 5 Reasons to Choose the Regis RCRM Program

  1. Choose from two specialty tracks: Regulatory Affairs and Clinical Research Management.
  2. Finish in as little as 16 months full-time.
  3. No program will work harder to provide you with internships and job placements with industry leaders to grow your professional network.
  4. Our flexible formats, including real-time virtual classroom, are the ideal combination of on-campus and online learning.
  5. Regis’ close proximity to Boston, the health care and medical research capital of the world, attracts innovative industry-active faculty who bring classroom teaching together with real-world applications.

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