Clinical Database Programmer

Responsibilities

• Develop, program, validate, and maintain clinical trial databases according to company and industry standards
• Maintain and contribute to the company library of standard CDASH compliant CRFs
• Act as the primary technical contact for the data management team on assigned studies
• Ensure high quality of programming and strict adherence to company standards

Requirements

• Bachelor's or Advanced degree in Life Sciences, Computer Science, or an equivalent field
• Minimum 5 years of Rave study build experience in a similar position within the Pharma or Healthcare sector
• Excellent verbal and written communication skills
• Meticulous attention to detail

Preferred Qualifications

• C# programming experience for custom functions
• Medidata Rave Study Builder certification
• Veeva EDC programming experience

Benefits

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

About the Company

Medpace is a full-service global Clinical Research Organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, we employ over 6,000 people across 40+ countries, dedicated to accelerating the development of safe and effective medical therapeutics.