UNIV - Research Program Coordinator II - Journeyman - Department of Neurosurgery
Listed on 2026-08-22
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Research/Development
Clinical Research, Research Scientist
Job Description
Summary:
The Research Program Coordinator II–Journeyman will lead and/or oversee the implementation and day‑to‑day operations of multiple complex research studies or a large research grant. They will be responsible for conducting all research related activities within a portfolio of assigned clinical trials. They also work directly with patients, study staff, Principal investigators and study sponsors to ensure institutional and Internal Review Board (IRB) compliance and that the integrity of the study is maintained.
Coordination and management of industry sponsored and investigator‑initiated trials involving subject screening, enrollment, data collection, scheduling visits, and conducting follow‑up visits. They are responsible for maintaining regulatory documents, logs, and reporting adverse events and protocol deviations to appropriate agencies. This candidate will serve as a research subject matter expert or resource across research domains and areas and will have the ability to train others on and apply research regulations to a variety of scenarios.
- 30% Review all research protocols, submissions, and all required documents for submission and approval. Prepare budgets for each project for submission to appropriate funding sources and the MUSC Office of Research Programs, so that they meet all IRB and FDA requirements. Coordinate and perform reporting and communications with the IRB, government agencies, and study sponsors regarding adverse effects, study implementations, renewals, terminations, close‑out and other activities necessary for exceptional performance of all studies from inception to close.
Responsible for the quality assurance of the assigned projects. Liaison between investigators, sub‑sites, and sponsors. - 25% Coordinate proper data management according to protocol requirements and compliance, collect and record all data pertaining to study patients on specific (funded or unfunded) studies and submit on time to research bases. Maintain up‑to‑date knowledge of the status of current studies. Review, evaluate, and report to PI on a monthly basis. Coordinate journals for references, assist in protocol development, dissemination of data, and data entry producing clean data as required by sponsors in a timely manner.
- 25% Liaison between the patient and the PI regarding consent forms for patient enrollment and for scheduling of treatments in conjunction with protocol timelines. Collaborate with all members of the research team to develop and implement strategies for the effective management of the research studies. Coordinate with nurses, tech, and other hospital services required for successful study milestones. Implement recruitment and enrollment strategy for the division.
Collaborate with other sub‑sites in enrollment productivity and assist Program Manager in handling multicenter trials. Communicate with sub‑sites about contractual agreements, start‑up site documents, training, and producing clean data. Work with Program Manager on conference development such as agenda, minutes, and other required documents for successful meetings. - 10% Continuously examine and evaluate the effects of the research regimen on study subjects and contribute to the advancement of services. Participate in department research activities as required and attend meetings and conferences mandated by the protocols.
- 5% Participate in writing and presentation of research reports and grant protocols. Actively pursue additional grant studies and sources of funding for continued salary support. Support Program Manager in newsletter or any correspondence to sub‑sites.
- 5% Review workload and operating procedures of each research study and determine priorities and workflow. Willing to travel and accept additional tasks as assigned by the Program Manager.
A bachelor's degree and three years of relevant program experience.
Physical Requirements(
Note:
The following descriptions are applicable to this section: Continuous - 6-8 hours per shift; Frequent - 2-6 hours per shift; Infrequent - 0-2 hours per shift) Ability to perform job functions in an upright position.…
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