Trial Master File Intern

Medpace•Cincinnati, OH

46d

About The Position

We are currently hiring full-time or part-time Spring and Summer 2025 interns for an exciting opportunity in clinical research managing our Trial Master File. The Trial Master File (TMF) is a collection of documentation that allows the conduct of a clinical trial, and the integrity of the data produced, to be evaluated by regulatory bodies, such as the FDA. The TMF is an important tool and can help teams manage trials more effectively. Therefore, TMF oversight is important to the successful execution of a trial and ultimately plays a big role in a new drug or device receiving approval by the FDA. In this position, you would be working with a highly experienced team of other administrators and clinical research professionals that can help you grow your skillset while working for a growing and developing company.

Requirements

High school diploma, or equivalent
High attention to detail
Excellent organizational skills
Strong written and verbal communication skills
Able to work a minimum of 20-24 hours a week.

Nice To Haves

Some experience in document administration preferred
Knowledge of MS Office and experience with MS Excel is preferred

Responsibilities

Manage electronic filing system for trial documentation
Track, maintain, and perform quality check of electronic documents
Communicate with internal associates globally regarding errors in trial documents
Prepare documents for shipment.