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Job #02755

About our client Our client is a reputable, privately held CRO that is experiencing unprecedented growth. The company has an experienced management team, a very high customer retention rate, industry low-employee turnover and a dedication to helping their staff maintain a strong work-life balance. This is a great opportunity for the right candidate! Position Location Clinical Research Associate (Home-Based) Midwestern USA Salary Highly competitive package, commensurate with experience Responsibilities 1) Implement clinical studies, study monitoring, study management and data management/reporting 2) Act as an efficient and experienced liaison between the study-site staff and company 3) Handle various tasks like preparing regulatory reports and clinical documents, creating study management tools and coordinating data collection/reporting with other departments (as required) 4) Assist in developing junior staff 5) Participate (proactively) in departmental programs Requirements 1) RN/BS in Biological Sciences or a related field (or equivalent combination of education and experience) 2) Minimum 3 years of CRA experience in monitoring clinical trials from qualification to closeout 3) 3+ years of experience in field monitoring 4) Knowledge and understanding of FDA regulations with their practical implementation and GCPs 5) Excellent problem-solving skills 6) Exceptional interpersonal and communication skills 7) Home-office with high-speed internet connection 8) ) Willingness to travel (up to 65%)