Associate Scientist Iii
CurrentCoordinates the bioanalytical analysis phase of regulated and non-regulated pre-clinical pharmaceutical studies with management, study directors, and clients to attain reliable analytical results.Maintains important client timelines regarding report submission and study completion.Communicates professionally and cordially with sponsors and clients in a timely manner to keep projects on track and to meet deadlines.Oversees laboratory technicians assigned to studies to achieve quality results and helps to guide, teach, and answer questions.Effectively develops biological matrix extraction procedures and LC-MS/MS analysis methods for various small molecule pharmaceutical compounds in method development and validation projects.Composes protocols, test methods, standard operating procedures, and reports.Responsible for different LC-MS/MS instruments and laboratory equipment and their general maintenance and troubleshooting as well as maintaining 5S workspace efficiency in different laboratories on-site.Addresses Quality Assurance audits of study data and reports to maintain high quality standards of data collection compliant with regulatory requirements.Organize inter-departmental themed food days to cultivate an environment of camaraderie and togetherness and to encourage culinary creativity.
