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Job #03524

About our client Our client is a well-established international research organization with its own oncology division. With its extensive background in clinical research and solid infrastructure (80 employees), our Client has the means to develop, manage and conduct a study in its entirety, ranging from a small phase I to large phase III trials. It is being recognized as one of the major networks in breast cancer clinical research with over 9,000 patients enrolled Position Location CRA Vancouver, BC Salary Highly competitive package, commensurate with experience Responsibilities 1) Conducting site visits (initiation, monitoring, termination) 2) Ensuring adherence to FDA and ICH-GCP regulations 3) Ensuring adherence to local regulations 4) Ensuring the completion and collection of regulatory documents 5) Instructing the site staff in their roles and responsibilities in conducting clinical trials 6) Evaluating and reporting site performance and protocol compliance 7) Performing data verification of source documents 8) Performing CRFs collection 9) Performing product accountability and supply tracking 10) Ensuring completion and collection of SAEs 11) Assisting with data validation and resolution of queries 12) Ensuring compliance with SOPs Requirements 1) Scientific background. (Research Nurse, Scientist, Pharmacist, BS, MS, PhD.) 2) 3+ years experience conducting site visits (initiation, monitoring, termination) 3) Knowledge in oncology would be a major asset 4) Rigorous, organized, autonomous, and self-motivated. 5) Good interpersonal communication skills, sense of prioritization, willing to travel in and around Los Angeles 60% 6) Able to work in a multi-cultural environment, Good computer knowledge (Word, Excel, Power Point)