Trial Master File Administrator

Responsibilities

• Manage the electronic filing system for trial documentation
• Track, maintain, and perform quality checks on electronic documents to ensure they meet established standards
• Communicate with internal associates globally regarding the Trial Master File (TMF)
• Prepare documents for shipment

Requirements

• Associates degree or equivalent
• Experience in document administration
• High attention to detail and exemplary organizational skills
• Strong written and verbal communication skills
• Proficiency in MS Office, specifically Excel and Outlook

Benefits

• Competitive compensation and benefits package
• Competitive PTO packages, starting at 20+ days
• Structured career paths with opportunities for professional growth
• Modern, eco-friendly campus with an on-site fitness center
• Employee health and wellness initiatives
• Company-sponsored employee appreciation events
• Discounts on local sports, fitness gyms, and attractions

About the Company

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs more than 6,000 people across 40+ countries, dedicated to accelerating the global development of safe and effective medical therapeutics.