UNIV - Program Coordinator I (Journeyman) - Department of Rehabilitation Sciences

Medical University of South Carolina
•$46,206 - $78,540

About The Position

The Department of Rehabilitation Sciences in the College of Health Professions at the Medical University of South Carolina is seeking a Research Program Coordinator I-Journeyman. The coordinator will oversee day-to-day operations for a federally funded, multi-site research study evaluating real-world dysarthria treatment outcomes for people with Parkinson disease. The study will enroll people with Parkinson disease, care partners, and speech-language pathologists from clinical sites across the United States. The coordinator will support clinical site onboarding and communication, recruitment, participant screening and consent, remote data-collection instructions, REDCap instruments and outcome tracking, data quality assurance, and regulatory documentation. The role also includes preparing study manuals and reports, attending focus group discussions and taking field notes, overseeing graduate student assistants, and serving as a central contact for participants, clinical partners, and collaborating research teams. Study activities must be carried out accurately and consistently in accordance with the protocol, IRB requirements, and institutional policies. Continued employment depends on satisfactory job performance and continued funding availability.

Requirements

  • Bachelor's degree.
  • Two years of relevant program experience.

Responsibilities

  • Coordinate day-to-day operations for a federally funded, multi-site research study on dysarthria treatment outcomes for people with Parkinson disease.
  • Support clinical site onboarding and communication.
  • Recruit participants and conduct eligibility screening and consent procedures.
  • Instruct participants on remote data-collection procedures.
  • Maintain REDCap instruments and track study outcomes.
  • Conduct data quality assurance and maintain regulatory documentation.
  • Prepare study manuals and reports.
  • Attend focus group discussions and take field notes.
  • Oversee graduate student assistants.
  • Serve as a central point of contact for participants, clinical partners, and collaborating research teams.
  • Help ensure study activities comply with the protocol, IRB requirements, and institutional policies.
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