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A company is looking for a Sr. Study Coordinator responsible for supporting clinical research and ensuring participant safety.
Key ResponsibilitiesSupport the screening process for potential participants and obtain informed consentManage investigational drug logistics and coordinate the patient's participation journey in the studyMonitor study adherence to protocols and maintain regulatory complianceRequired Qualifications and EducationLicensed Practical Nurse or equivalent license in the state of practiceMinimum 2 years of study coordinator experienceStrong understanding of Good Clinical Practice (GCP) and research ethicsProficient in Microsoft Office Suite and electronic medical record (EMR) systemsAbility to work flexible schedules, including 24 / 7 on-call coverage
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