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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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questions, consenting and enrolling participants onto research studies, 2) coordinating study activities: tracking patient referrals, screening patients for eligibility, scheduling study visits and procedures
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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
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allocating patient stipends. May be asked to assist with research scheduling. Maintain complete, well-organized, and audit-ready study and participant files (e.g., subject charts, case report forms, enrollment
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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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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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equipment at the end of each day. This position is part-time, with a work schedule from Monday to Friday, typically from 9:00 AM to 3:00 PM, with potential early drop-off and late pick-up responsibilities
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needed. This position will require the research nurse to have a variable schedule. Research participants are seen in the clinical setting during early morning, daytime, and early evening hours. Position
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certifications or licenses are strongly preferred. The schedule is primarily Monday through Friday during normal business hours. However, the position will require some weekend work on a rotational basis and must