Clinical Trial Assistant

Responsibilities

• Provide day-to-day departmental and project support, including managing study supply inventory, orders, shipping, and filing
• Coordinate and provide minutes for department or project meetings and conference calls
• Conduct quality reviews of documents to ensure accuracy
• Maintain databases and spreadsheets and compile regular reports
• Perform other administrative tasks as needed to support the Site Contracts team

Requirements

• Bachelor’s degree, preferably in Life Sciences
• Fluency in the English language
• Strong organizational and prioritization skills
• Proficiency in Microsoft Office
• Excellent attention to detail and strong oral and written communication skills
• Previous experience in an office setting is preferred

Benefits

• Competitive compensation and benefits package
• Competitive PTO packages
• Flexible work environment
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

About the Company

Medpace is a full-service clinical research organization (CRO) providing 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 a scientific and disciplined approach. Headquartered in Cincinnati, Ohio, we employ more than 5,000 people across 40+ countries.