Responsibilities
- Write statistical programs for use in creating analysis datasets, tables, listings, and figures;
- Review analysis plans for appropriate methods;
- Program study analyses and review study results;
- Communicate the project requirements for cleanup and data capture to ensure the key study variables are suitable for analysis.
Qualifications
- Master’s Degree in Statistics/Biostatistics required;
- SAS and/or statistical programming experience;
- Knowledge of databases and data management processes;
- Knowledge of statistical methods commonly used in pharmaceutical clinical trials.
Travel
Minimal
Location
Must relocate to Cincinnati, OH
Benefits
- Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with local nonprofit organizations
- Discounts on local sports games, fitness gyms, and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Structured career paths with opportunities for professional growth
- Discounted tuition for UC online programs
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries and providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.