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Summer Intern, Records Management

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Arrowhead Pharmaceuticals, Inc

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Location:
United States , Verona

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Contract Type:
Not provided

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Salary:

23.00 USD / Hour

Job Description:

The Records Management Intern will support information governance efforts at Arrowhead Pharmaceuticals by assisting with the organization, maintenance, and digitization of physical and electronic records. This internship offers hands-on experience in records management, archival systems, and compliance-related documentation within a regulated pharmaceutical environment. The intern’s work will help improve efficiency, accessibility, and accuracy of critical records while supporting regulatory and retention requirements.

Job Responsibility:

  • Assist with organizing, cataloging, and indexing physical and digital records to support effective records management and archival practices
  • Maintain accurate archival inventories, ensuring records are properly tracked and easily retrievable
  • Support the conversion of physical documents to digital formats, including scanning, uploading, tagging, and applying appropriate metadata
  • Help implement, update, and maintain digital archival systems in accordance with company standards
  • Verify that digital records comply with naming conventions, storage requirements, and data integrity guidelines
  • Assist with compliance and regulatory recordkeeping activities, including applying and updating records retention schedules
  • Support staff with archival backlog, scanning, and organizational tasks to improve operational efficiency

Requirements:

  • Currently enrolled student at an accredited university or college pursuing a Master’s Degree in Information Management, Library Science, Records Management, Archives, Business Administration, Life Sciences, or a related discipline
  • Basic familiarity with document management, recordkeeping, or archival concepts through coursework, training, or prior experience
  • Strong organizational skills with attention to detail and accuracy
  • Basic computer proficiency, including experience with Microsoft Office or similar productivity tools
  • Ability to follow established procedures, naming conventions, and compliance-related guidelines
  • Effective written and verbal communication skills and ability to work collaboratively

Nice to have:

  • Coursework or hands-on experience in records management, archives, information governance, or quality systems
  • Familiarity with digital document management or electronic records systems (e.g., document repositories, archival databases, eDMS platforms)
  • Experience scanning, digitizing, or organizing large volumes of documents
  • Basic understanding of regulatory or compliance frameworks in regulated environments (e.g., GLP, GxP, FDA)
  • Strong attention to detail with the ability to identify inconsistencies in documentation or file organization
  • Interest in quality assurance, compliance, or information lifecycle management within a scientific or pharmaceutical setting
What we offer:

competitive salaries and an excellent benefit package

Additional Information:

Job Posted:
February 12, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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