Clinical Research Coordinator
صاحب العمل نشط
حالة تأهب وظيفة
سيتم تحديثك بأحدث تنبيهات الوظائف عبر البريد الإلكتروني
شارك هذه الوظيفة
حالة تأهب وظيفة
سيتم تحديثك بأحدث تنبيهات الوظائف عبر البريد الإلكتروني
لم يكشف
لم يتم الكشف عن الراتب
الوصف الوظيفي
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.
-
Association of Clinical Research Professionals Certified Professional (ACRPCP)
-
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
-
MultiDisciplinary 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.
نوع التوظيف
دوام كامل
