Under the supervision of a Clinical Research Supervisor or Principal Investigator (PI), the Assistant Clinical Research Coordinator supports research efforts for a multi-center pragmatic randomized clinical trial to reduce post-discharge surgical site infection. The incumbent will perform entry-level duties related to the support and coordination of clinical studies and may receive training and development to prepare and advance for journey-level work at the next level within the series.
Key responsibilities include duties related to recruitment and coordination, including creating training and educational documents, data collection tools, protocols, recruitment or protocol scripts, surveys, recruitment flyer distribution and other trial related preparatory documents. It also includes coordinating meetings with key surgeons and hospital staff, including scheduling, and pulling together agenda and content as requested by the Principal Investigating team. Additional responsibilities include data entry and creation of figures and graphs, and providing IRB support for drafts, submissions, modifications and progress reports. Duties will include interfacing with collaborators at participating sites. Support of project activities may include travel to recruitment and follow up locations to ensure accurate conduct and progress. Such activities may include completing follow up surveys and conducting chart reviews/redaction. . All vaccines and health screening required for employees who have presence in hospitals and patient areas will be required, including, but not limited to influenza, COVID, TDap, chicken pox, MMR, TB, and hepatitis.The final salary and offer components are subject to additional approvals based on UC policy.
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