Project Coordinator, Data Monitoring - Entry Level
US-OH-Cincinnati
US Careers
Req #: 12810
Type: Full-Time
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Overview: 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. Responsibilities: * Provide administrative, logistical, and coordinating support for Data Monitoring Committees (DMCs), including scheduling meetings, distributing unblinded data, and documenting decisions and outcomes * Partner with the Internal Medpace team to identify and contract independent physicians and industry experts to assemble DMCs to review of safety and efficacy data for ongoing trials * Assist in the development and maintenance of study specific documents describing DMC processes and procedures * Maintain the study blind and handle unblinded materials with discretion to ensure confidentiality * May be responsible for other projects and responsibilities as assigned Qualifications: * Bachelor's degree in life science or health related field; * Excellent written and verbal communication skills; * Proficient knowledge of Microsoft Word, Excel, and PowerPoint; and * Exposure to/knowledge of medical terminology and healthcare systems
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