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Job #02684

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) Western USA Salary Highly competitive package, commensurate with experience Responsibilities 1) Handle implementation of clinical studies along with study monitoring, study management and data management/reporting 2) Act as an efficient and experienced liaison between the study site staff and company 3) Prepare regulatory reports, clinical documents and create study management tools 4) Coordinate data collection/reporting with other departments 5) Assist in the development of junior staff 6) Initiate participation in department programs Requirements 1) RN/BS degree in Biological Sciences/related field (or equivalent combination of education and experience) 2) Minimum 5 years of CRA experience in monitoring clinical trials from qualification to closeout 3) Experience in monitoring cardiovascular trials 4) At least 3 years of experience in field monitoring 5) Experience in Cardiology preferred 6) Superb knowledge and understanding of FDA regulations and GCPs along with their practical implementation 7) Excellent problem-solving skills 8) Exceptional interpersonal and communication skills 9) Willingness to travel – up to 65% (overnight)