Job Description
Location: IC: NINDS Street: 10 Center Dr Bldg: 10Room: 7D38 City: BethesdaState & Zip:MD 20814
Weekly Hours - FT: 30-40 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.
Association of Clinical Research Professionals Certified Professional (ACRP-CP)
Association of Clinical Research Professionals (ACRP)
Certified Clinical Research Professional (CCRP)
Certified Clinical Research Coordinator (CCRC)
Certified Clinical Research Associate (CCRA
Miscellaneous Health Medical Professions
Nursing
Community and Public Health
General Medical and Health Services
Neuroscience
Miscellaneous Biology
Cognitive Science and Biopsychology
Biology
Genetics
Health and Medical Preparatory Programs
Nutrition Sciences
Pharmacy
Pharmaceutical Sciences and Administration
Treatment Therapy Professions
Communication Disorders Sciences and Services
Sociology
Miscellaneous Social Sciences
Interdisciplinary Social Sciences
General Social Sciences
Miscellaneous Psychology
Clinical Psychology
Psychology
Social Psychology
Social Work
Chemistry
Multi-Disciplinary or General Science
- Clinical Trial Management System (CTMS)
- Electronic Medical Records System
- Electronic Data Capture System
Overseeing and documenting IP dispensing, inventory and reconciliation
Closing clinical trial sites down on completion of clinical trial
Ordering, tracking, and managing IP and trial materials
Implementation of clinical trial site action plans
Training clinical trial site staff
Coordinating project meetings
Previous clinical trial work
Electronic medical records
Protocol review revision Phase I or II experience
Patient confidentiality
Remote site monitoring
Regulatory compliance
Protocol development
Clinical Research
Protocol writing
Clinical Trials
Data Monitoring
Data Integrity
Patient care
Recruitment
Scheduling
Screening
Research
ICH/GCP
SOPs
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.