Job Description
This position involves working in Respiratory Research at the Respiratory Institute. Responsibilities include managing regulatory tasks, data entry, monitoring visits, and conducting patient visits. Initially, the coordinator will shadow and observe patient visits, then gradually handle 1-3 visits per week independently. Patient visits can take up to a full day. Additional duties include electronic medical record (EMR) documentation using Epic, billing compliance data entry, and handling queries. The coordinator will manage regulatory binders, CV and license tracking, and Institutional Review Board (IRB) submissions. Monitoring visits involve coordinating with CRO/Sponsors, setting up visits, arranging meetings, and preparing necessary documentation. Data entry will be performed using systems like Medidata and Epic. The role also involves screening patients for study eligibility and managing inclusion/exclusion criteria.
Hard SkillsClinical research experiencePatient consentingRegulatory managementInclusion and exclusion criteriaData managementSoft SkillsAttention to detailStrong organizational skillsExcellent communicationEmpathy and compassionTeam collaborationJob Type
This is a Contract-to-Hire position with a duration of 12 Month(s).
Work Site
This is a hybrid position requiring some days on-site in Cleveland, Ohio and some days remote.
Work Environment
Some flexibility to work from home one day a week after 90 days of onboarding and demonstrated independence. Onsite work is at the main campus, with parking costs to be covered by the employee.
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