Description
Summary of Qualifications Detail-oriented, enthusiastic, and highly motivated Research Professional with 19+ years of successful experience. Diverse background encompasses research, laboratory analysis, reporting, and project/study planning and execution experience. Skilled at ensuring compliance with Standard Operating Procedures (SOP), Good Clinical Practices (GCP), and applicable policies and regulations. In-depth knowledge of ICH GCP guidelines. Possesses finely-honed analytical, communication, problem solving, critical thinking, and leadership skills. Currently seeking a position which will effectively utilize all acquired skills, abilities, and areas of expertise as follows: Analytical Method Development Research/Development Study & Testing Methods Project/Study Planning Process Analysis/Improvement Workplace/Lab Safety Data Compilation/Analysis Protocol/Regulatory Compliance Record/File Maintenance Report Generation ICH-GCP, FDA Laboratory Instrumentation Quality Control (QC) Sample/Inventory Management Team Collaboration Policy/SOP Compliance Drug/Toxicology Analysis Applied Chemistry
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