Field all initial patient phone screenings and input/regularly update all patient information into the patient database in order to ensure the most accurate database possible
Pre-screen potential study participants via telephone or email inquiry and schedule appropriate patients for screening visits to consent in a timely manner
Educate and address questions from potential study participants as needed to ensure they understand the logistics of the clinical study and their role as a volunteer.
Coordinate with CRC’s and effectively schedule new patient screening visits;
Bachelor’s degree in health sciences or related field required & at least 3 years of clinical research experience.
Must be able to function independently, possess exceptional time management and interpersonal communication skills, as well as the ability to multi-task.
Internal Number: 101
About Clinical Trials of South Carolina
Our mission is to safely advance science and improve lives through quality-driven research, collaboration and innovation. As an independent investigative site located in Charleston, SC, Clinical Trials of South Carolina conducts top-level research studies across multiple therapeutic areas.