Project Coordinator, Data Monitoring

Responsibilities

• Provide administrative, logistical, and coordinating support for Data Monitoring Committees (DMCs), including scheduling meetings and documenting outcomes
• Distribute unblinded data and maintain the study blind with high discretion to ensure confidentiality
• Partner with the Internal Medpace team to identify and contract independent physicians and industry experts for DMC assembly
• Assist in the development and maintenance of study-specific documents describing DMC processes and procedures
• Handle unblinded materials and manage other projects as assigned

Requirements

• Bachelor's degree in a life science or health-related field
• Excellent written and verbal communication skills
• Proficient knowledge of Microsoft Word, Excel, and PowerPoint
• Exposure to or knowledge of medical terminology and healthcare systems

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
• 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, we leverage local regulatory and therapeutic expertise to accelerate the global development of safe and effective medical therapeutics.