Clinical Research Specialist

Prepare to work in a clinical research environment by learning clinical trial structure, key regulatory requirements that govern clinical trial execution and collection/analysis of clinical trial data. This program covers basic knowledge of clinical research concepts and structure, how to conduct clinical trials, how to navigate the regulatory requirements for successful trial completion and the fundamentals of working with clinical trial data.

The Certified Clinical Research Professional (CCRP) Exam, offered through the Society of Clinical Research Associates (SOCRA), is available for students who have existing Associates or Bachelor's degree in science or other health related field and/or work experience in clinical research.

Pre-Requisites
Students should be proficient in keyboarding, have a basic understanding of a word-processing computer program (Microsoft Word recommended), and have a command of English grammar and punctuation. A science background is recommended, but not required.

Program Outline
This program has 1 class:

Register for each course separately

CTR 3110A3 Healthcare Clinical Research Specialist (108 hours)

Contact Hours: 108 Hours

Industry-recognized credential: Society of Clinical Research Associates (SOCRA)

Complete in: 6 month or less

For non-credit student support services or to see if you qualify for financial assistance, contact the Career Pathways Program & Student Resources. 

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Course Details & Registration Information
 

Pathways to Launching a Clinical Research CareerHRD-3004BN21 available classes
This course explores employment opportunities in clinical research that support the development of new, innovative treatments. You’ll learn about the roles of researchers, research assistants, data managers, and monitors and coordinators – and find out why this industry is e...
Healthcare Clinical Research SpecialistCTR-3110A3
This comprehensive course prepares students to conduct clinical trials successfully. It covers fundamental clinical research concepts as well as how to structure and execute a clinical trial, navigate regulatory requirements, and collect and analyze clinical trial data. Stud...
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