Delivers lectures and hands-on demonstrations covering topics such as signal acquisition, sensor technology, and data analysis. Develops and grades lab assignments and projects focused on real-world biomedical applications, aligning with industry and academic standards. Guides students through the use of software tools such as LabVIEW and Arduino IDE for biomedical signal processing and instrumentation tasks.

Mentors undergraduate students on neuromuscular biomechanics projects, enhancing collaboration, problem-solving skills, and interdisciplinary research in the lab. Experienced in marker-based motion capture (Motion Analysis, Vicon), marker-less motion capture (Qualysis, OpenCap), electromyography (Delsys), fNIRS (NIRSport), and Visual3D. Develops custom MATLAB and R scripts for data processing and analysis.

Managed and hired staff in the clinical trials department, ensuring smooth and efficient operations. Developed and implemented Standard Operating Procedures and workflows to optimize department performance while supporting physician-research partnerships and fostering connections across Boys Town's clinics and laboratories. Collaborated with industry pharmaceutical and medical device companies to coordinate and execute clinical trials, ensuring compliance with regulatory standards and enhancing research outcomes.

Facilitated connections between researchers and physicians through a collaboration mechanism titled the 'Innovation Accelerator' and oversaw clinical trial operations. Assisted principal investigators with trial related communications internally and externally with the Institutional Review Board and Grant Accounting staff. Established workflow processes for clinical trials and collaborated with researchers and physicians in Neurodevelopment, Genetics, Movement, Microbiome, Neuroimaging, and Audiology.

Assisted the principal investigator with clinical trial administration, including data collection, regulatory compliance, and scheduling of study-related activities. Managed study recruitment, follow-up with research subjects, and ensured adherence to Good Clinical Practice (GCP) documentation principles. Interacted with subjects and maintained compliance with study protocols and regulatory requirements.