PROFESSIONAL SUMMARY Eight years of clinical experience of coordinating and implementing activities related to clinical research Highly skilled in conducting analysis of performance monitoring data to bring about comprehension of equity impact Hands on experience in designing and developing data collection instruments and systems related to diseases on case-based surveillance Proven experience of assisting in planning implementing electronic reporting Reviewed Quality Assurance Unit (QAU) audits of study documents Clinical Trial Studies Phase I/II and Phase IV RELEVANT QUALIFICATIONS Knowledge of infectious diseases, cancer and public health Excellent understanding of epidemiological principles and surveillance methodologies Understanding of clinical research methods Excellent oral and written communication skills Proficiency in developing and maintaining databases
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