毒理学总监

Primarily responsible for clinical pathology data interpretation and development related new capability establishment. Duties include but are not limited to supervision of and participation in the following:Responsible for ensuring the quality, accuracy, and integrity of clinical examination analysis data. Provide professional analysis advice and interpret analysis results, assisting the Study Director (SD) in interpreting clinical examination data. Ensure the data analysis process adheres to the laboratory’s quality control standards. Participate in training and development activities to enhance data analysis skills and knowledge.Proficient in operating various clinical examination instruments and equipment, ensuring their normal operation. Identify and resolve issues and system alerts related to equipment operation, quickly addressing problems to ensure the smooth conduct of experiments.Responsible for analyzing and evaluating clinical pathology data and writing clinical pathology reports. Write reports based on data analysis results, ensuring the content is scientific, accurate, and clear. Collaborate with relevant teams or departments to ensure timely submission of data and reports.Responsible for evaluating bone marrow smears, blood smears, reticulocyte smears, and urine morphology examinations. Write bone marrow smear evaluation reports based on examination results, collaborating with relevant teams or departments to ensure timely submission of data and reports.Responsible for developing new projects based on new molecular types and customer needs, establishing new capabilities in clinical examination analysis. Track the latest industry technologies and trends, developing and expanding new capabilities.Timely identification of potential problems or anomalies, conducting in-depth analysis to find the root cause, including issues related to technology, processes, or equipment. Promote process optimization and efficiency improvement to reduce the frequency and impact of problems.KEY RESPONSIBILITIESDescription Proficient in conducting clinical pathology laboratory analyses in toxicology studies carried out in GLP facilities.Understand and adhere to GLP principles, familiar with the basic principles and requirements of GLP to ensure laboratory operations comply with these standards. Participate in laboratory quality control and quality assurance procedures to ensure the accuracy and reliability of experimental results meet these standards, and assist in internal audits and inspections.Provide technical support, and expertise for the new capability study design, analysis of data, and interpretation of results.Assure on-time delivery of high-quality new capabilities projects.Provide leadership and training to technical staff as requiredMINIMUM REQUIREMENTSPhD degree or equal of clinical pathology laboratory science, biopharmaceuticals, or other pharmaceutical sciences and with DACVP certification.At least 5-10-year industry experience.Fluent in English, both in writing and oral communication.