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Clinical Research Protocol Specialist
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Patient Research Nurse Coordinator
2 months ago
Job Description
Job Title:
Patient Research Nurse Coordinator
Location:
Bethesda, Maryland
Weekly Hours:
Full Time (30-40 hours per week)
Overall Position Summary and Objectives:
We are seeking a dedicated and experienced Patient Research Nurse Coordinator to join our clinical research team in Bethesda, Maryland. The incumbent will play a crucial role in executing the full scope of clinical research nursing, which includes providing care to research participants and supporting study implementation, data collection, and ensuring human subject protection. The position is situated within a dynamic clinical research program area that serves multiple admitting institutes and a diverse patient population. Responsibilities will extend across various programs and units, potentially including community outreach.
Minimum Education:
Bachelor's degree in Nursing
Certifications & Licenses:
BLS/CPR certification
Registered Nurse (RN) license
Key Skills:
Maintain client communication regarding data management project status and review key project questions with clients, working in a hospital setting
Patient/Family education
Process, track, and validate data accurately and on time, in accordance with data processing and entry instructions
Perform data abstraction and data entry on several different protocols into multiple clinical research databases
Strong writing skills, particularly in clinical research
Prepare, review, and submit clinical data to monitoring agencies
Software:
Proficiency with Electronic Medical Records (EMR) systems
Field of Study:
Nursing
Key Responsibilities:
Assist physicians and research staff with patient data collection.
Update databases related to study activities.
Recruit and schedule subjects, including both normal controls and patients.
Ensure all medical reports are completed and informed consent is signed in time for patient meetings.
Prepare and mail study materials to participants.
Analyze, update, and monitor databases related to study activities.
Independently recruit and schedule subjects, both normal controls and patients.
Participate in periodic meetings to discuss research activities.
Join our team and contribute to ground-breaking clinical research while providing exceptional care and support to our research participants. If you are passionate about clinical research and meet the qualifications listed, we encourage you to apply.
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