Min Mo Email & Phone Number

Columbus, Ohio, United States

• Tracks and maintains up-to-date, accurate data related to a variety of nonclinical study activities and/or research operations projects
• Provides information to drive cross-functional communication, data-driven decision making, prioritization, and successful execution of multiple nonclinical studies concurrently
• In close collaboration with the Program Management group, ensures knowledge of milestones, timelines, and deliverables for research programs and utilizes this information to guide scheduling and execution of.
• Builds relationships with key stakeholders
• Lead meetings related to ongoing projects and/or assist in meeting material preparation and dissemination of meeting agendas and meeting summaries
• Identifies opportunities for improvement of processes and efficient use of resources

Columbus, Ohio Area

• Lead research projects in a broad range of scientific areas, including cell assay development, therapeutic and diagnostic product development and optimization, bioanalytical method development, qualification and.
• Create experimental designs and study protocols for the GLP compliant and non-GLP compliant studies; oversee data collection, data analysis and keeping all related documentations; coordinate with the scientific team to.
• Review method development data, validation and bioanalytical reports
• Supervise the research team to ensure the contracted projects meet the timeline and budget
• Coordinate with the Quality Assurance Unit (QAU) and the lab manager to ensure the studies adherence to GLP (FDA 21 CFR Part 58) compliance

Columbus, OH

• Coordinate with team members to make sure that all parties are on track with project requirements, deadlines, and schedules
• Meet with project team members to identify and resolve issues
• Prepare and submit project deliverables and ensure that they adhere to quality standards
• Prepare status reports by gathering, analyzing and summarizing relevant information
• Coordinate the development of SOPs, protocols, training materials and other documents as needed to enable successful implementation of the project
• Coordinate with the QA department to review QSDs, SOPs, associated logs and forms to ensure the project was performed as GLP-compliant standards, maintain proper records in accordance with SOPs and policies

Columbus, OH

• Design, execute experiments and analyze data to present progress to clients in a regular basis
• Design, express, purify and characterize various recombinant human enzymes for intracellular enzyme replacement therapy
• Develop cell-based assays
• Direct potency assays development for dendritic-based immunotherapy

Columbus, OH

• Screen and characterize monoclonal antibodies from hybridoma clones to target antigens
• Identify variable regions of heavy chain/light chain from hybridoma clones for detection of antigens via antibody engineering
• Transfect and clone hybridoma cells for antigen detection
• Construct, produce and site-specifically mutate a single chain antibody for radioimmunotherapy
• Express a variety of recombinant antibodies in mammalian cells by using Lentivirus vectors

Rockville, MD

• Establish a Baculovirus expression system to express a variety of immunological molecules
• Engineer high-affinity T cell receptor/cytokine fusion for therapeutic targeting

Doctor Of Philosophy (Ph.D.), Biochemistry And Molecular Biology

Bachelor'S Degree, Medical Clinical Sciences/Graduate Medical Studies