Records Management Analyst I
About The Position
This position supports our customer, the Food and Drug Administration (FDA) by responding to inquiries and processing electronic applications and documentation in accordance with established Standard Operating Procedures (SOPs) and business rules. The Records Management Specialist I (Editor) primarily processes electronic documents using multiple systems. While assigned to specific core functions, individuals will be cross trained to perform additional duties based on operational needs. Work Location: Onsite – Landover, MD Schedule: Monday through Friday, 8:30 AM – 5:00 PM Security Clearance: Must possess or be able to obtain a Public Trust Clearance.
Requirements
- High School Diploma required; Bachelor’s degree preferred.
- Three (3) years of related experience, including:
- Two (2) years of direct document processing experience
- At least one (1) year of office, records, or computer-based work experience
- Ability to type 40 words per minute with no more than two errors.
- Proficiency in Microsoft Office and other office automation tools.
- Familiarity with medical terminology and HIPAA regulations is required.
- Strong data entry skills with exceptional attention to detail.
- Excellent proofreading skills with the ability to identify errors in spelling, grammar, and punctuation.
- Strong analytical, organizational, and written communication skills.
- Ability to maintain accuracy and productivity in a high-volume environment.
Responsibilities
- Process electronic documents in accordance with current SOPs and quality standards.
- Apply appropriate procedures and interpret business rules within established guidelines.
- Perform Medical Device Reporting (MDR) support activities, including:
- Proofreading documents for grammar, spelling, and punctuation
- Editing for clarity and accuracy
- Redacting confidential patient and manufacturer information in accordance with FOIA exemptions
- Review Adverse Event Reports involving:
- Injury or fatality related to medical devices
- Reports submitted by healthcare providers or emergency personnel
- Documentation submitted to the FDA for regulatory review
- Ensure all redactions and revisions comply with federal privacy and disclosure requirements.
- Maintain high productivity and accuracy in a fast-paced electronic production environment.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
