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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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scheduling. Maintain complete, well-organized, and audit-ready study and participant files (e.g., subject charts, case report forms, enrollment logs, hospital records, etc.) from participant screening through
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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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- 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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. 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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the quality of the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing study protocol training. The CRC is also responsible
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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