Medical University of South Carolina-posted 3 days ago
Full-time • Manager
Charleston, SC
5,001-10,000 employees

A full-time Program Manager I is needed to continue successful execution and oversight of our SC ECHO cohort in the Department of Public Health Sciences and the Department of Obstetrics and Gynecology. This position will include co-directing and managing ECHO project initiatives and research studies by overseeing and contributing to program design, implementation, and daily administrative activities. This role combines direct clinical-research interface with strategic program oversight. The Program Manager will be responsible for maintaining regulatory requirements, enrollment, study procedures, data collection and management, and supervision of team members. The Program Manager will also be responsible for contributing to the daily activities of the study including recruitment of study participants, conducting study visits, processing samples, maintaining stakeholder relationships, and training staff to perform these activities. The Program Manager will work with clinicians, patients, families, and researchers in the clinical setting and interact with the national ECHO Coordinating Center, the national ECHO Data Center, and the national ECHO Biorepository.

  • Responsible for defining study deliverables, contributing to study deliverables, and managing to a timeline.
  • Directing workflow, participating in workflow, and providing feedback to team to ensure study goals are met including screening, recruitment, enrollment, data collection, retention and community outreach for the study.
  • Responsible for the budgeting of the clinical components of the project.
  • Co-lead the coordination and implementation of the ECHO program at MUSC.
  • Supervision of research staff and their training according to National ECHO Guidelines.
  • Oversee regulatory documentation for all IRB submissions and study sponsor.
  • A bachelor's degree and three years relevant program experience.
  • Five years’ experience related to observational cohort studies, experience with participant recruitment and community outreach, and familiarity with MUSC’s IRB processes and regulatory requirements.
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