临床监查员CA求职英文简历模版.doc

XXXXX DOB: MMM.YYYY Gender: Male Native place: XXXXX city, XXXXX Province Major: Clinical Medicine Molecular Oncology Phone: 139XXXXXXXX Email: XXXXXXXX Objective Senior CRA or CRA II (located in Shanghai) Summary Certified CRA of ACRP, March 2011~May 31, 2013; More than two years experiences as a Clinical Research Associate; In-depth knowledge of Helsinki Declaration, ICH-GCP Guidelines and SOPs; Self-study of FDA CFR online; Therapeutic areas include cancer, endocrine and cardiovascular diseases; Good understanding of medical terminology; Familiarity with EDC, IVRS/IWRS and central laboratory procedures; Excellent interpersonal skills and fast prioritization of tasks; Strong sense of self-discipline; Good spirit of team work; Fluent in American English and Mandarin; Enjoy travelling. Education 2005~2008, Master; Biomedical researches on Molecular Oncology; Fudan University, Shanghai, China 2000~2005, Bachelor; Clinical Medicine; University of South China Work Experience I. Mar/2011-June/2011, Research Assistant at Buck Institute for Research on Aging Job Description: Assist in the design, preparation, implementation of experiments, and analysis of the results to explore the compounds that can extend lifespan of animal models and their corresponding molecular mechanisms, as well as to find new strategies for the treatment of neuron degenerative diseases such as Alzheimer’s disease and Parkinson’s disease; Acquired a well understanding of American culture and improved communication skills in English through this job. II. Sep/2010-Mar/2011, Member of Association of Clinical Research Professional (ACRP) (1) Systematically learning of ICH-E6, ICH-E8, ICH-E2A and ACRP recommended documents, such as Guide to Clinical Trials; (2) Passed the examination of Certified Clinical Research Associate (CCRA); (3) Study the clinical trial regulations of Food and Drug Administration (FDA); (4) Involved in the discussion of monitoring and management of clinical trials in th