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WH

Medical Records Specialist- Gettysburg- Days

WellSpan Health·Gettysburg, Pennsylvania

Full Time·On Site·0-2 yrs·Posted 5 days ago
Practice for this role

About the role

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Collects, analyzes, and processes patient medical information. Ensures the completeness and accuracy of all clinical documentation.

General Summary

Collects, analyzes and processes patient medical information to ensure the completeness and accuracy of clinical documentation.

Requirements

Requires a High School Diploma or GED and less than one year of relevant experience. Preferred qualifications include coursework in medical terminology, anatomy, and physiology.

  • high school
  • Medical Terminology
  • Microsoft Office Suite
  • Clinical Documentation
  • Microsoft Outlook
  • Anatomy
  • Medical Records Management
  • Physiology

Benefits

  • Paid Time Off (PTO)
  • Retirement Savings Plan
  • Education Assistance
  • Comprehensive Health Benefits
  • Expanded Paid Parental Leave
  • Financial Education And Support

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
0-2 yrs
Location
Gettysburg, Pennsylvania
Posted
Jul 23, 2026
Application
Employer website
WH

Hiring organization

WellSpan Health

WellSpan Health is hiring in Gettysburg, Pennsylvania. It operates in medical practices. Team size: 2-10 employees. Headquarters: York, Pennsylvania. This opening is listed as full_time.

Salary listed on 4 jobs
IndustryMedical Practices
Size2-10 employees
HQYork, Pennsylvania
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Market context

Clinical research coordinator roles in Pennsylvania

In Pennsylvania, administration roles tied to clinical research often draw steady demand from hospitals, universities, and research sites that need coordinators who can keep studies organized and compliant. These roles are competitive because employers look for candidates with direct coordinator experience, strong Microsoft Office skills, and practical clinical abilities such as phlebotomy or a willingness to train quickly. Review the AI-summarized requirements and benefits here to save time, then confirm your experience matches the study setting and be ready to discuss how you handle documentation and participant coordination.

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