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Northwestern Offers Clinical Research and Regulatory Administration Graduate Certificate Program

CHICAGO, Feb. 5 /PRNewswire-USNewswire/ -- In response to the growing need for competent industry professionals, Northwestern University has created a graduate certificate program in Clinical Research and Regulatory Administration

Northwestern University School of Continuing Studies (SCS), in partnership with Northwestern University Clinical and Translational Sciences Institute (NUCATS), will launch the new program this spring with a Feb. 22, 2008, application deadline and a March 31, 2008, program start date. Applications accepted for fall start as well.

The four-course, graduate certificate curriculum grounds professionals in the key concepts of the clinical research enterprise and allows them to focus in one of two research areas: regulatory affairs and administration, or clinical trials design and conduct. The program enables research professionals to develop competency at the site and clinical operations levels.

Program Outcomes

At the conclusion of the graduate certificate, students will have demonstrated expertise in:

-- Understanding the current regulatory environment in clinical research,

-- Interpreting regulatory requirements and applying them to various roles in the clinical research and drug/device development process,

-- Creating systems and processes to assure quality research outcomes, and

-- Fostering a climate of excellence in clinical research and research and regulatory administration.

Industry Outlook

Career advancement opportunities abound for the effective clinical research professional at academic medical centers, research sites, and in pharmaceutical and medical device organizations.

Recent growth in clinical and translational research has heightened the need for a competent clinical research work force in industry and academia. While government organizations re-engineer the clinical research enterprise and ensure compliance with federal regulations, pharmaceutical companies seek to improve the breadth and efficiency of clinical research and maintain quality and safety standards. As a result, pharmaceutical companies and research sites must ensure that the research process is safe, efficient, and compliant. There is also focus on bringing much-needed products to market in a reasonable time frame to improve patient health. These requirements demand a highly skilled clinical research team with a knowledge and skill base surrounding clinical trial management, implementation, compliance, and regulatory affairs.

Northwestern University School of Continuing Studies offers working professionals the opportunity to continue their education through flexible evening programs. Visit for more information regarding programs and schedules for graduate and undergraduate degree and professional development certificate programs.

SOURCE Northwestern University
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