Full-Time

Univ – Program Coordinator I

Advanced, Department of Medicine: Division of Rheumatology

Posted on 11/21/2024

Medical University of South Carolina

Medical University of South Carolina

Compensation Overview

$39k - $72.1kAnnually

Mid

Charleston, SC, USA

Category
Healthcare Administration & Support
Medical, Clinical & Veterinary
Requirements
  • A bachelor's degree and three years of relevant program experience.
  • A bachelor's degree in biology, nursing and other natural, life, or health care field is preferred.
  • Background in education and/or community outreach will also be considered.
  • Ability to think critically, proactively address potential issues and solutions, and effectively manage time and tasks through exceptional organizational skills.
  • Ability to exercise judgment and discretion.
  • Ability to effectively communicate (both written and verbally).
  • Excellent interpersonal skills.
  • Ability to present a professional demeanor.
Responsibilities
  • 35% - Visit Coordination: Efficiently coordinate assigned lupus clinical research studies including interacting with study participants, physicians, SCTR Nexus, Investigational Drug Services, Sponsors/Clinical Research Organizations and other MUSC clinical departments as appropriate. Activities include the recruitment of study participants, protocol implementation (scheduling/execution of study visit schedule of assessments), and related documentation of study participation. Inventories supplies and equipment of the protocol to avoid delays in protocol execution. Some work on lesser holidays can be expected to meet the prioritized needs of our study participants.
  • 30% - Data Management: Coordinate data collection of all study related participant documentation within appropriate case report forms. Includes collection of prospective data as well as extraction from existing records review. Completion of applicable data entry of participant assessments into designated research records/electronic databases.
  • 15% - Compliance: Executes studies so that they are carried out according to Code of Federal Regulations, Good Clinical Practices, and MUSC policies for human research. Addresses all regulatory needs/submissions with the proper oversight board (local &/or central IRBs and other agencies as applicable) carrying out submissions and reporting needs as needed for appropriate document management. Coordinates communication and visitation with study collaborators and monitors, following up with monitoring findings and meets all discrepancies and clarification needs.
  • 10% - Miscellaneous: Participate in Divisional outreach activities to assist with study recruitment and general team goals of community engagement and education. Occasional need to include travel and afterhours/weekend work flexibility to accommodate community activities and events.
  • 5% - Administrative: The Program Coordinator will assist with and work closely with the Investigators and Program Manager in assisting with administrative aspects for assigned trials and projects. Maintain good communication and effective working relationships with faculty/investigators, supervisor/program manager, fellow coordinators, and the business office.
  • 5% - Other duties as required - which may include additional travel (i.e. MUSC clinical satellites or investigator meetings) to prioritize and ensure participant safety and data integrity.
Medical University of South Carolina

Medical University of South Carolina

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