Clinical Trial Site Relationship Coordinator

• Provide ongoing support of sites, including identifying and discussing future new business opportunities and feasibility assessments;
• Develop effective plans for site contact and follow-up;
• Support management in expediting feasibility, site selection and study start-up;
• Communication with PI and investigative sites; and
• May be responsible for other projects and responsibilities as assigned.

• Minimum a Bachelor of Science in health-related field;
• Previous experience as CRA/Study coordinator or Study nurse in German Sites is required;
• Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines preferred;
• Knowledge of medical terminology and clinical patient management preferred;
• Fluency in bothGermanand English;
• Demonstrated organizational and prioritization skills;
• Excellent oral and written communication skills; and
• Proficient knowledge of Microsoft Office applications.

Medpace is a full-service clinical contract research organization (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.