Clinical Research Regulatory Coordinator-CEDAS
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Job Location:
Chapel Hill, NC - USA
Monthly Salary:
$ 53000 - 65000
Posted on:
3 hours ago
Vacancies:
1 Vacancy
Job Summary
Position Summary
This position will serve as a Clinical Research Regulatory Coordinator within the Center for Gastrointestinal Biology and Disease. The Clinical Research Participant Regulatory Coordinator is responsible for research regulatory management for a variety of complex clinical research protocols including leading efforts in creating gathering editing compiling and reporting regulatory information. The Clinical Research Regulatory Coordinator will analyze and reconcile information from various sources to complete various regulatory based tasks such as Institutional Review Board submissions and applications management creation and maintenance of regulatory files and quality assurance activities.
Required Qualifications Competencies And Experience
Must be able to use considerable judgement and skills in performing work assignments. Strong written and verbal communication skills. Must be able to work and communicate with diverse populations effectively and professionally. Ability to work independently as well as function as part of a team. Proficient with Microsoft Outlook Excel and Word.
Preferred Qualifications Competencies And Experience
Experience independently coordinating clinical trials with direct experience in eRegulatory systems (Veeva SiteVault Florence etc.)
Work Schedule
Monday-Friday 8am-5pm other times as needed
This position will serve as a Clinical Research Regulatory Coordinator within the Center for Gastrointestinal Biology and Disease. The Clinical Research Participant Regulatory Coordinator is responsible for research regulatory management for a variety of complex clinical research protocols including leading efforts in creating gathering editing compiling and reporting regulatory information. The Clinical Research Regulatory Coordinator will analyze and reconcile information from various sources to complete various regulatory based tasks such as Institutional Review Board submissions and applications management creation and maintenance of regulatory files and quality assurance activities.
Required Qualifications Competencies And Experience
Must be able to use considerable judgement and skills in performing work assignments. Strong written and verbal communication skills. Must be able to work and communicate with diverse populations effectively and professionally. Ability to work independently as well as function as part of a team. Proficient with Microsoft Outlook Excel and Word.
Preferred Qualifications Competencies And Experience
Experience independently coordinating clinical trials with direct experience in eRegulatory systems (Veeva SiteVault Florence etc.)
Work Schedule
Monday-Friday 8am-5pm other times as needed
Required Experience:
Staff IC
Key Skills
- CSS
- Cloud Computing
- Health Education
- Actuary
- Building Electrician
About Company
The University of North Carolina at Chapel Hill, the nation’s first public university, is a global higher education leader known for innovative teaching, research and public service. A member of the prestigious Association of American Universities, Carolina regularly ranks as the best ... View more
