M.S. in Clinical Research Administration

The need for trained clinical research administrators is growing. Walden’s M.S. in Clinical Research Administration provides students with the knowledge and skills required for effective clinical research administration and management, including a detailed understanding of the regulatory environment.

A leading provider of online health education within the United States, Walden has developed an M.S. in Clinical Research Administration that draws on the knowledge and insights of experts in the field, resulting in a curriculum that is fully aligned with the latest practices in clinical research administration and management and that informs students of the regulatory guidelines of the U.S. Food and Drug Administration (FDA) and comparable agencies abroad.

This program offers

A relevant, comprehensive curriculum—including texts, interactive media, and practical experiences—designed to provide insight into the most recent developments in the clinical research field
An emphasis on state-of-the-art knowledge of clinical research execution and management through analysis of the day-to-day operations in clinical testing activities
A practicum to give students hands-on experience in the field
A capstone that provides an opportunity for students to complete a professional online portfolio showcasing their work
Active mentoring from Walden faculty members and a range of support services from our staff

Completion Requirements

36 semester credits
- Core courses (30 sem. cr.)
- Practicum and capstone (6 sem. cr.)
ePortfolio
Minimum 3 semester credits per 8-week term enrollment

Estimated time to completion of 2 years. Time to completion may vary by student, depending on individual progress and credits transferred. For a personalized estimate of your time to completion, call your enrollment advisor at 1-866-492-5336.

Curriculum

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

Course Code	Course Title	Credits
	Semester 1
CLRA 6100	Introduction to Clinical Research	3
CLRA 6115	Pathophysiological Basis of Clinical Research	3
	Semester 2
CLRA 6130	Ethical, Legal, and Regulatory Considerations in Clinical Investigations	3
CLRA 6145	Design and Conduct of the Clinical Protocol	3
	Semester 3
CLRA 6160	Good Clinical Practice (GCP) in Managing and Monitoring Clinical Trials	3
CLRA 6175	Biostatistics	3
	Semester 4
CLRA 6190	Information and Data Management	3
CLRA 6205	Product Development in the Pharmaceutical, Biotechnology, and Medical Device Industries	3
	Semester 5
CLRA 6220	Health Economics and Financial Management in Clinical Research Administration	3
CLRA 6235	Epidemiology	3
	Semester 6
CLRA 6550	Practicum	3
CLRA 6560	Capstone	3