Clinical Research Specialist
The Research Triangle region is a global hub for clinical research activities. Become part of this vibrant industry by preparing to work as a clinical research monitor or clinical trials associate. The program covers the fundamentals of monitoring clinical trials, including the regulatory requirements for monitoring, how to conduct site visits and how to report findings to sponsors.
The program is online, and all hours will be completed via Blackboard, where assignments and learning materials will be available for students to complete from their computer at their own pace. There are no scheduled meeting times for classes.
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.
The Certified Clinical Research Professional exam, offered through the Society of Clinical Research Associates, is available for individuals who meet any of the following criteria:
- Have two years of experience as a full-time clinical research professional (or have 3,500 hours part-time) during the last five years
- Hold an associate, undergraduate or graduate degree in clinical research and have at least one year of full-time experience (or 1,750 hours part-time) as a clinical research professional during the past two years
- Hold an undergraduate or graduate certificate in clinical research with at least 12 credit hours of study, or a total of at least 144 credit hours, from a community college, college or university and hold an associate or bachelor's degree in a science, health science, pharmacy or related field and have at least one year of full-time experience (or 1,750 hours part-time) as a clinical research professional during the past two years
Industry-recognized credential: Society of Clinical Research Associates
Complete in: Six months or less
Financial assistance available
Workforce Continuing Education offers financial assistance for many workforce training programs through the Propel program and other resources. Email [email protected] for more information.
Clinical Research Specialist Courses
Healthcare Clinical Research Specialist
Course ID: CTR-3110A3 | Overview
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. Students will be able to apply their skills for employment in a clinical research environment such as a clinical trial site or contract research organization.
| Section | Start Date | End Date | Location | Instructor | Price | Open Seats | |
|---|---|---|---|---|---|---|---|
| 303104 | Online | Mainhart | 180.00 | 24 | Register | ||
| 303209 | Online | Harris | 180.00 | 25 | Register |
If you would like to be notified when additional sections become available, please use Wake Tech's Notify Me service.
Pathways to Launching a Clinical Research Career
Course ID: HRD-3004BN2 | Overview
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 expected to grow. You’ll also learn about clinical research employers with job openings. You’ll be prepared to enter the clinical research field with an understanding of the professional organizations and certifications needed for advancement.
No active courses available at this time.
To be notified when this course becomes available, please use
Wake Tech's Notify Me service.
Monitoring Clinical Trials
Course ID: CTR-3110B3 | Overview
The Research Triangle Park is world headquarters for clinical research activities. Become part of this vibrant industry by preparing to work as a clinical research monitor or clinical trials associate. This course covers the fundamentals of monitoring clinical trials, including the regulatory requirements for monitoring, how to conduct site visits, and how to report findings to sponsors.
| Section | Start Date | End Date | Location | Instructor | Price | Open Seats | |
|---|---|---|---|---|---|---|---|
| 302095 | Online | Pope | 180.00 | 22 | Register |
If you would like to be notified when additional sections become available, please use Wake Tech's Notify Me service.
Coordinating Clinical Research: The Role of the Clinical Research Coordinator
Course ID: CTR-3110C3 | Overview
The Triangle area of North Carolina is world headquarters for clinical research activities. In addition to the local pharmaceutical companies that call NC home, the area includes large operations of the world’s top contract research organizations (CROs) including IQVIA, PPD, Parexel, ICON, and Syneos.
One of the principal job roles for the industry is the clinical research coordinator (CRC). CRCs work at sites conducting clinical trials. Sites include Duke University, UNC-Chapel Hill, Wake Research Associates, as well as other smaller, independently owned research sites. CRCs work with doctors and other medical staff who conduct clinical trials on behalf of pharmaceutical and medical device companies.
This course provides training on the fundamentals of coordinating clinical research studies including regulatory requirements for adverse event reporting, data management, and subject safety. CRCs are in great demand. This course provides training for those who wish to transition into this role.
| Section | Start Date | End Date | Location | Instructor | Price | Open Seats | |
|---|---|---|---|---|---|---|---|
| 302267 | Online | Pope | 180.00 | 22 | Register |
If you would like to be notified when additional sections become available, please use Wake Tech's Notify Me service.
