Clinical Research Coordinator
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Not Disclosed
Salary Not Disclosed
Job Description
Location: IC: NINDS Street: 10 Center Dr Bldg: 10 Room: 7D38 City: Bethesda State & Zip: MD 20814
Weekly Hours FT: 3040 hours per week
The primary role for this Research Coordinator (RC) position is to provide clinical research coordination and protocol navigation for the NINDS Intramural Research Program.
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Association of Clinical Research Professionals Certified Professional (ACRPCP)
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Association of Clinical Research Professionals (ACRP)
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Certified Clinical Research Professional (CCRP)
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Certified Clinical Research Coordinator (CCRC)
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Certified Clinical Research Associate (CCRA
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Miscellaneous Health Medical Professions
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Nursing
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Community and Public Health
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General Medical and Health Services
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Neuroscience
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Miscellaneous Biology
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Cognitive Science and Biopsychology
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Biology
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Genetics
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Health and Medical Preparatory Programs
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Nutrition Sciences
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Pharmacy
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Pharmaceutical Sciences and Administration
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Treatment Therapy Professions
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Communication Disorders Sciences and Services
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Sociology
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Miscellaneous Social Sciences
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Interdisciplinary Social Sciences
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General Social Sciences
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Miscellaneous Psychology
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Clinical Psychology
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Psychology
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Social Psychology
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Social Work
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Chemistry
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MultiDisciplinary or General Science
- Clinical Trial Management System (CTMS)
- Electronic Medical Records System
- Electronic Data Capture System
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Overseeing and documenting IP dispensing inventory and reconciliation
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Closing clinical trial sites down on completion of clinical trial
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Ordering tracking and managing IP and trial materials
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Implementation of clinical trial site action plans
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Training clinical trial site staff
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Coordinating project meetings
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Previous clinical trial work
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Electronic medical records
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Protocol review revision Phase I or II experience
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Patient confidentiality
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Remote site monitoring
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Regulatory compliance
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Protocol development
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Clinical Research
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Protocol writing
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Clinical Trials
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Data Monitoring
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Data Integrity
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Patient care
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Recruitment
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Scheduling
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Screening
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Research
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ICH/GCP
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SOPs
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Liaising with regulatory authorities
Statement of Work Details
Supports clinical staff develop implement and maintain clinical research data files and materials.
- Assist preparing and submitting for review accurate source documents related to all research procedures.
Employment Type
Full Time
