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Job #03371

About our client Our client is a diagnostics company based in California. With facilities in more than 60 countries worldwide, they offer products and services used by the industry to assist with the diagnosis, treatment and management of infectious diseases. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. Position Location Senior Clinical Research Associate California Salary Highly competitive package, commensurate with experience Responsibilities 1) Oversee the day-to-day administration of clinical trials 2) Monitor activities at the clinical study site including study initiation, interim monitoring and closeout visits 3) Prepare clinical documentation (training materials, data forms, study manuals, etc.) 4) Establish and maintain strong relationships with study coordinators 5) Assist with site training (GCPs, protocol, product implant, etc.) 6) Ensure routine communications with the site regarding status/resolution of study queries 7) Maintain clinical files 8) Ensure clinical file documents are updated frequently 9) Liaise with data management CRO 10) Track the status of data entry and data lock Requirements 1) BS in a Health or scientifically-related field 2) Minimum 3 years of experience as a Clinical Research Monitor/Associate in the medical device industry or in drug/biologic trials 3) Background in clinical research and medical terminology 4) Familiarity with clinical research data entry 5) Proficiency in Windows and MS Office 6) Excellent project management and communication (written and oral) skills 7) Strong analytical, planning, interpersonal and organizational skills 8) Strong initiative and ability to work with minimal supervision as well as multi-task 9) Proven attention to detail and accuracy 10) Flexible and creative individual