Regulatory Affairs Assistant
IQVIA
full-time
Posted on:
Location Type: Office
Location: Fairfax • Virginia • United States
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About the role
- Facilitate document flow for clinical trials at NEXT Oncology.
- Maintain official regulatory files and ensure timely distribution of study documents.
- Enter and maintain study-specific information in internal databases.
- Distribute new/updated study documents and IRB review/approval documents.
- Set up Site Initiation Visits and meetings as required.
- Attend meetings and perform a variety of administrative duties.
Requirements
- Bachelor's degree in administration or science.
- At least three years of experience in Regulatory Affairs in a research setting.
- Proficiency in Microsoft Word and Adobe Acrobat.
- Excellent verbal and written communication skills.
Benefits
- Excellent customer service to all internal and external customers.
- Opportunities for professional growth and development.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
Regulatory AffairsDocument ManagementDatabase Management
Soft skills
CommunicationOrganizational SkillsAdministrative Skills
Certifications
Bachelor's Degree