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Clinical Research Administration – (M.Sc.)

Application Deadline: no application deadlines
Location: Amsterdam / Netherlands / View location on map ▾ Hide location on map ▴
Duration: 36 months Start Date: October
Educational Form:
  • Taught
Education Variants:
  • Fulltime
  • Online education
Credits (ECTS): 180
Languages: English 

Location of Laureate Online Education in Cooperation with Walden University

Throughout the history of clinical trials, research professionals have been a critical part of medical breakthroughs that have improved the lives of millions of people. But there are still great strides to be made toward safer and more reliable treatments for genetic disorders and diseases such as breast cancer, diabetes, and heart disease. Walden’s Master of Science in Clinical Research Administration program can prepare you for key roles managing and monitoring life-changing clinical research phases and processes. This program focuses on the latest technologies, the safest methods for testing, the protection of human subjects, and the hope that drives all medical advancements.

Coursework in such areas as product development, the business of clinical research, epidemiology, and good clinical practice are designed to broaden your understanding of the process that produces innovative, high-impact clinical research products. Gain an understanding of the legal, regulatory, and ethical concerns that govern clinical research, as well as historical controversies and triumphs that have defined medical product development. Grow your professional network with faculty who are subject matter experts from diverse fields, including medicine, law, nursing, and business.

This scholar-practitioner program offers:

  • A unique combination of in-depth research, interactive media, discussion, and practical experiences that can enable you to gain knowledge and skills to apply immediately in your work.
  • Insight into how developments in the field change lives and improve patient care.
  • Analysis of day-to-day operations in clinical trial activities.
  • An optional practicum that offers hands-on experience in the field.
  • A basic understanding of clinical research ethics and the regulatory environment.

Contents

The program’s courses are delivered in a prescribed sequence.

Semester 1

  • Introduction to Clinical Research
  • Pathophysiological Basis of Clinical Research

Semester 2

  • Ethical, Legal, and Regulatory Considerations in Clinical Investigations
  • Design and Conduct of the Clinical Protocol

Semester 3

  • Good Clinical Practice (GCP) in Managing and Monitoring Clinical Trials
  • Biostatistics

Semester 4

  • Information and Data Management
  • Product Development in the Pharmaceutical, Biotechnology, and Medical Device Industries

Semester 5

  • Health Economics and Financial Management in Clinical Research Administration
  • Epidemiology

Semester 6

  • Capstone

You are normally required to take an English Proficiency Test if you come from a non-English speaking country.

Most European Universities recognise the IELTS test.

More information

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Requirements

A bachelor’s degree or higher

Additional Requirements

Minimal degree required: Bachelor's degree
Minimal amount of work experience Not specified

Accreditation

Walden is accredited by The Higher Learning Commission and a member of the North Central Association, www.ncahlc.org. The North Central Association is one of the six regional accrediting associations recognized by the U.S. Department of Education and the Council for Higher Education Accreditation (CHEA).


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