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Job #03378

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 Southern California Salary Highly competitive package, commensurate with experience Responsibilities 1) Oversee the implementation of clinical studies, study monitoring and management as well as data management/reporting 2) Serve as an efficient and experienced liaison between the study site staff and the company 3) Prepare regulatory reports and clinical documents 4) Create study management tools 5) Coordinate data collection/reporting with other departments Requirements 1) RN or BS in Biological Sciences or a related field (or an equivalent combination of education and experience) 2) 5+ years of CRA experience in monitoring clinical trials (from qualification to closeout) 3) Experience in monitoring oncology trials 4) Strong knowledge and understanding of FDA regulations and GCPs along with their practical implementation 5) Expertise in assisting in the development of junior staff and the initiative to participate in departmental programs 6) Exceptional interpersonal, problem-solving and communication (written and oral) skills 7) Willingness to travel regionally (up to 65%)