Clinical Records Administrator

4 weeks ago


Cincinnati, Ohio, United States Medpace Full time

We are seeking a detail-oriented and organized Clinical Records Administrator to join our team at Medpace. In this role, you will be responsible for ensuring the integrity of our Trial Master File (TMF) by managing electronic documents, tracking and maintaining quality checks, and communicating with internal associates globally.

Responsibilities:
  • Manage electronic filing system for trial documentation
  • Track, maintain, and perform quality check of electronic documents
  • Communicate with internal associates globally regarding the TMF
  • Prepare documents for shipment
Qualifications:
  • High school diploma or equivalent
  • Experience in document administration
  • High attention to detail
  • Exemplary organizational skills
  • Strong written and verbal communication skills
  • Knowledge of MS Office (Excel and Outlook)

Medpace is a full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.

As a Clinical Records Administrator at Medpace, you will have the opportunity to work with a team of experienced professionals and contribute to the success of our clinical trials. If you are a detail-oriented and organized individual with a passion for document administration, we encourage you to apply for this exciting opportunity.



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