Clinical Trial Assistant
US-OH-Cincinnati
US Careers
Req #: 10637
Type: Full-Time
|
|
|||||||||||
|
||||||||||||
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: * Perform administrative duties in conformity with company policies and procedures; * Provide day-to-day study support activities such as maintenence of project-related files, corresponding with study teams, etc. * Coordinate and schedule meetings, provide meeting minutes; * Maintain databases/project specific status reports * Support filing and quality control reviews of our internal regulatory filing system; * Manage study supplies; * Perform other administrative tasks as needed Qualifications: * A high school diploma or equivalent; * Proficient in English; * At least 2 years of administrative experience, preferably in a health care field; * Attention to detail, and excellent organizational and prioritization skills; * High functioning knowledge of and experience with Microsoft Office programs is required; and * Excellent oral and written communication skills.
Share this job:
