Review all corrective action by lower-level roles and follow-up with directors on findings. Monitor daily workflows of team and process samples meticulously to avoid cross-contamination. Monitor and meet established turn-around-time deadlines for clinical testing. Assist supervisor/directors to ensure all routine maintenance of laboratory equipment is performed as required. Effectively communicate with laboratory members, investigators, physicians, stakeholders, including Executive and Advisory Board members, to ensure seamless communication and act as designee in scientific meetings as needed. Ensures accurate recording of relevant data and values in case folders and internal databases. Direct documentation according to CAP/CLIA and institutional SOPs. Review to ensure complete and accurate logging of sample receipt, aliquoting, and storage in the LIMS to maintain traceability across all omics workflows. Assist Medical Director and team to accurately and precisely analyze molecular assay results for final interpretation by medical staff. Adhere to established laboratory and hospital policies and good clinical laboratory practice in areas of procedures, quality control, quality assurance and safety and compliance. Oversee all technical aspects of research and clinical projects, participate in and review new assay development plans. rain new lab members and/or sign off on competency documents. Demonstrate and set an example for excellent organizational skills and time management to process large batches of samples efficiently while maintaining accuracy and compliance under strict turnaround-time requirements. Assist Lab Management by contributing and at times perform as designee on all cross-platform QA/QC efforts, ensuring harmonization of standards across genomics, proteomics, and metabolomics workflows.