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- Systematically track treatment response and monitor patients (in person or phone) for changes in clinical symptoms and treatment side effects or complications- Participate in regularly scheduled caseload
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documents. · Communicate with study team members and regulatory review boards. · Recruit, consent and screen patients according to protocol. · Schedule patient visits and any necessary
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with prospective students and to schedule individual or group advising sessions on your personal calendar. Each advising session includes a review of the candidate's credentials, a 15-minute call, and a
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; participating in professional societies To date, clinical hours are Monday through Friday 8:30AM – 5:30PM; flexibility in scheduling is required for all positions Contributes to team effort by accomplishing and
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protocols by review of study protocol, related literature prior to study start date. Schedule and conduct follow-up visits with patients and ensure all follow-up activities are conducted within protocol
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enroll potential study subjects from inpatient, outpatient and emergency room; participate in the conduct of audits; process and ship blood, stool and specimens; schedule patient visits and any necessary
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. Provide executive administrative support, including managing physicians’ Outlook calendars, coordinate meetings, schedule conference calls and research team meetings, submit reimbursements from physicians
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. Conduct taste preference assessments and computerized behavioral assessments with children. 2) Organize and Conduct Study Visits: Set up, schedule, and complete tasks associated with all screening and study
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of biological samples require extreme flexibility within the daily work schedule. This position reports directly to the study's project manager. This position may require flexibility to work occasional nights
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and specimens; schedule patient visits and any necessary testing; obtain records required to complete case report forms; conduct initiation, monitoring and closeout visits with Sponsor or CRO; adhere