Frequently Asked Questions

What are the benefits of a Master of Science in Clinical Research and Regulatory Administration?
Pharmaceutical companies must pass all new drugs through several phases of human clinical trials to demonstrate to the FDA the drugs are safe and effective for the condition or disease area they are intended to treat. Pharmaceutical companies commission physicians at academic medical centers, clinical research organizations, and clinical sites to conduct the necessary trials.

The Master of Science in Clinical Research and Regulatory Administration prepares individuals for many different clinical research roles, including: Business Development and Operations; Clinical Operations; Clinical Research Coordination; Clinical Data Management; Medical Writing; Clinical Research Monitoring; Pharmaceutical Sales; Project Management; and Clinical Regulatory Affairs.

I have already taken a course from the Clinical and Translational Sciences Institute. Do I have to apply for admission to the program, and will I need to repeat the course?
All students must apply for admission to the program. Students who have completed the Pathways in Clinical Research CRA/CRC Training course (fall 2004 or later) or the Essentials of Initiating Clinical Research course (fall 2007 or later), may petition to substitute an approved elective course for the core course Essentials of Initiating Clinical Research.

What kind of background is required for admission?
Students include those looking to enter the clinical research industry and those seeking to enhance their professional development. Many students already possess graduate or professional degrees including RNs, PhDs, MDs, MBAs, PharmDs, NPs, and other specialized degrees. However, a background in nursing or healthcare is not required. Applicants must have a minimum of a bachelor's degree (BS, BA, BSN or other) and relevant work experience. Please see the admission section of this website for a complete list of admission requirements.

Who are the course instructors?
Course instructors are Northwestern University faculty and industry experts with knowledge in clinical research and regulatory affairs administration. Nationally-recognized experts in the field participate as guest speakers.

What are the typical course requirements?
Each course includes lecture, discussion, and guest presentations. Readings include textbooks and recent literature. Students will be required to complete group projects, individual assignments, and/or exams.

Is financial aid available?
For information about financial aid, please visit: http://www.northwestern.edu/sfs/school_specifics/scs_grad.html. You should also make sure to check with your employer regarding possible tuition benefits.