UNIV - Program Coordinator II (Novice) - Department of Health Sciences and Research
About The Position
The Research Program Coordinator II (Novice) in the Department of Health Sciences and Research within MUSC’s College of Health Professions coordinates the day-to-day operations of multiple clinical and translational research studies focused on neurological rehabilitation, participant-centered interventions, and community-engaged research. The role develops operational systems across studies and provides guidance to other research staff. The coordinator works with principal investigators, research staff, collaborators, community partners, and study participants to support study implementation. Duties include participant recruitment and retention, informed consent, study visit coordination, regulatory compliance, database development and management, data collection and quality assurance, project tracking, and research reporting. The position calls for an organized, self-directed professional with strong written and verbal communication skills, the ability to work in remote and in-person environments, and the capacity to learn new technologies and research methodologies.
Requirements
- Bachelor’s degree.
- Two years of relevant program experience.
- Strong written and verbal communication skills.
- Ability to work effectively in remote and in-person environments.
- Demonstrated capacity to learn new technologies and research methodologies.
- Ability to meet the physical requirements described in the posting, including frequent seated, upright, and mobile work; indoor work; fine motor tasks; and occasional lifting, carrying, lowering, and pushing or pulling objects up to 15 pounds.
Responsibilities
- Coordinate day-to-day operations of multiple clinical and translational research studies.
- Develop operational systems across multiple studies.
- Provide guidance to other research staff.
- Work with principal investigators, research staff, collaborators, community partners, and study participants to support study implementation.
- Recruit and retain participants.
- Conduct informed consent procedures and coordinate study visits.
- Ensure regulatory compliance.
- Develop and manage databases.
- Collect data and conduct quality assurance.
- Track projects and prepare research reports.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
