Leonie Lyu

Carrying out selection, initiation, monitoring, and close-out visits at the participating clinical trial centres Developing study procedures, methodologies, and instructions for clinical trial staff, as well as design data collection tools Collecting, verifying, and finalising collected data to create reports and present results to medical staff Ensure the safety and well-being of test subjects by liaising with ethics committees; Submission of clinical trial documents for review and approval by EC

 Analysing product information for legal compliance, complete assessments, and perform regulatory compliance related tasks to completion  Preparing product registrations/filings and programme preparation in accordance with local guidance and practices  Tracking and managing product post-market response data and designing evaluation metrics to assess legal compliance

 High-throughput screening, biocatalysis, and the topic of plastic degradation  Proficiency in PCR, HPLC, MC, protein purification, transformation, fluorescence microscopy, and computer simulation