Job Summary
A company is looking for an Administrative Assistant - Regulatory Affairs to maintain regulatory documentation for investigational drug studies.
Key Responsibilities
- Maintain the Investigator Site File (ISF) for assigned studies, including IRB submissions and approvals
- Manage documentation and obtain Investigator signatures for study-specific documents
- Handle monitor visits and manage training documentation for study staff
Required Qualifications
- High school diploma or equivalent
- Proficient working knowledge of Microsoft Word
- Strong organizational skills and ability to complete tasks with minimal supervision
- Detail-oriented with good spelling, composition, and proofreading skills
- Ability to understand instructions and compose reports and correspondence
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