Research Assistant
About The Position
This temporary position will serve as a Regulatory Document Specialist within the department of Global Health and Infectious Diseases. The Regulatory Document Specialist is responsible for research regulatory management for a variety of complex clinical research protocols, including leading efforts in gathering, editing, compiling, and reporting regulatory information. The position will analyze and reconcile information from various sources to complete various regulatory based tasks, such as creation and maintenance of study regulatory files, maintenance of essential documents, leading and taking minutes for study team meetings, and quality assurance activities.
Requirements
- Experience in research regulatory management.
- Ability to gather, edit, compile, and report regulatory information.
- Skills in analyzing and reconciling information from various sources.
- Experience in creating and maintaining study regulatory files.
- Experience in maintaining essential documents.
- Ability to lead study team meetings and take minutes.
- Experience in quality assurance activities.
Responsibilities
- Gathering, editing, compiling, and reporting regulatory information for complex clinical research protocols.
- Analyzing and reconciling information from various sources to complete regulatory tasks.
- Creation and maintenance of study regulatory files.
- Maintenance of essential documents.
- Leading and taking minutes for study team meetings.
- Performing quality assurance activities.
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What This Job Offers
Career Level
Entry Level
Education Level
No Education Listed
