Full-Time

Uiv – Research Program Coordinator I

Psychiatry: Brain Stimulation Laboratory

Posted on 11/21/2024

Medical University of South Carolina

Medical University of South Carolina

Compensation Overview

$39k - $72.1kAnnually

Entry, Junior

Charleston, SC, USA

Position requires on-campus presence.

Category
Healthcare Administration & Support
Medical, Clinical & Veterinary
Required Skills
R
MATLAB
Requirements
  • A bachelor's degree and one year of relevant program experience.
  • A bachelor’s degree in Psychology, Neuroscience, Biology, Engineering, Computer Science or related field is preferred.
  • Prior experience in research is helpful but not mandatory.
  • Prior experience with EEG, fMRI or other physiological measures as well as TMS or other brain stimulation techniques is preferred but not mandatory.
  • The ability to use computer word and data processing programs including but not limited to Microsoft Office, MATLAB, R, and SPSS are very helpful.
Responsibilities
  • This individual will assist with recruitment and screening of research participants, including the development of advertising materials, meeting with and calling potential participants, distribution of advertising materials, and collaborating with relevant providers and researchers.
  • This individual will obtain informed consent, enroll study participants, conduct study visits as per the protocols and provide education information to subjects.
  • This individual will assist with non-invasive brain stimulation sessions.
  • This individual will conduct study visits before and after regular working hours when necessary to accommodate the schedules of subjects, MRI availability, etc.
  • This individual will coordinate proper data management collection according to protocol requirements and compliance. This individual will maintain behavioral, diagnostic, and EEG/fMRI/physiological data.
  • This individual will conduct data retrieval from large databases for data reporting and analysis.
  • This individual will initiate and maintain accurate and comprehensive records as required by the FDA, the IRB, the sponsors and Good Clinical Practice Guidelines. This individual will schedule and participate in all sponsor and/or IRB monitoring visits to review study protocols and collected data.
  • This individual will attend weekly staff meetings to review study progress.
Medical University of South Carolina

Medical University of South Carolina

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