Principal Duties and Responsibilities General Duties and ResponsibilitiesSubmitting regulatory documents to IRB and SponsorSubmitting the clinical study agreement to OSP for reviewAttending investigator meeting(s)Preparing for study initiationRecruitment of subjectsScreening and scheduling subjectsGetting voluntary subject consentTeaching subjects about protocol expectations for themPerforming study/protocol procedures in a detailed, accurate mannerMaintaining study filesTracking subjects, avoiding lost-to-follow-upDocumenting an adverse event, including:describing the eventseverity and frequencytreatmentresolutionProcessing and shipping lab workDesired Skills and ExperienceQualifications and Skills Bachelor’s degree or equivalent experience in a related field, with a minimum of 2 years of relevant experience.Fluency in English requiredOncology preferred but not required
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