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.
Minimum requirements - 1 Year - Research experience in at least one of the following areas: pharmaceutical, academic, device, NIH, investigator-initiated studies or registry trials.
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 or Bachelor Degree in a science and 3 years direct experience in that field.
Other Required Experience
International Air Transport Association Certification - Preferred
As South Carolina’s largest private, non-profit healthcare system, and second-largest private company, we are here to create a better state of health for South Carolinians. Prisma Health is inspired to help people live their healthiest lives. As the most comprehensive integrated healthcare system in South Carolina, we’re on a journey to transform the healthcare experience for our patients and their families. That’s why our team members are dedicated to living our purpose: Inspire health. Serve with compassion. Be the difference.