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Job #02960

About our client Our client is a global diagnostics company based in San Diego. They are a worldwide leader in the development, manufacturing and marketing of molecular diagnostics products used to diagnose human diseases and screen donated human blood. The company has a world-class management team, a strong product pipeline and a solid employee base of 1000 professionals. Position Location Clinical Research Scientist San Diego, California Salary Highly competitive package, commensurate with experience Responsibilities 1) Oversee scientific aspects of multiple clinical trials (protocol, study design, statistical plan, data analysis, report writing and publications) 2) Work with multiple teams to ensure coordination and acquisition of data, reviewing of results and preparation of reports 3) Assist with establishing as well as implementing policies and procedures (related to clinical trials) 4) Develop data model and data-analysis plan for multiple trials 5) Review, assess and interpret data from ongoing as well as completed trials 6) Identify study results that require additional testing and oversee testing 7) Provide scientific input and assist in developing clinical plans, protocols, reports and manuscripts 8) Work on extremely complex problems (analysis of situations or data involving evaluation of intangible variables) 9) Ensure continuous improvement of data collection and retrieval processes 10) Evaluate current systems and identify ways to improve efficiency 11) Make recommendations, identify opportunities and lead efforts to develop scientific abstracts, presentations as well as manuscripts for publication 12) Evaluate alternative systems 13) Provide materials and reports for reviewing by outside departments in advance of clinical report drafts 14) Exercise independent judgment in developing methods, techniques and evaluation criteria for obtaining results Requirements 1) BS/BA and minimum 10 – 12 years of related experience (or MS with 8 years of experience or Ph. D. with 6 years of related experience) 2) In-depth knowledge of clinical trial databases 3) Knowledge of statistics to apply and understand appropriate data analysis for clinical trials