This position is full-time, 8am-5pm M-F


Responsible for the implementation, management and oversight of clinical trial research studies including the education of research staff, healthcare team member, participants and their caregivers. Registers, compiles, submits and oversees clinical data, monitors study compliance and maintains a system for effective data flow for patients on clinical trials.  Manages patient visits and implements protocol related procedures.  Responsible for monitoring and communicating study participant progress and safety issues with the investigators, applicable regulatory agencies, health care team and study staff. 

Supervisory/Management ResponsibilitiesThis is a non-management job that will report to a supervisor, manager, director or executive.Minimum Education

Other - Associate degree in Allied Health OR Bachelor's Degree in health sciences or business.

Minimum Experience

1 Year - Research experience in at least one of the following areas:  pharmaceutical, academic, device, NIH, investigator initiated studies or registry trials.

Required Certifications/Registrations/LicensesNOT APPLICABLESpecific Acceptable Credentials (if applicable)

If Allied Health Degree: South Carolina certification/license in field. 

In lieu of the Above Minimum Requirements

The following requirements will also be considered in lieu of 1 year research experience:

Associate Degree in Allied Health plus 3 years direct experience in that field 


Bachelor Degree in a science and 3 years direct experience in that field.

Other Required Experience

International Air Transport Association Certification - Preferred

Position Posting Category

Clinical Professional/Technical

Greenville, SC 29607, US