Review and analyze Periodic Safety Update Reports and Periodic Benefit Risk Evaluation Reports.Review case reports on adverse reactions to drugs and vaccines.Causality assessment of adverse reactions to drugs and vaccines.

Coordinate research studies with inside and outside vendors (e.g., clinicians, professors, etc.) for the company. Maintain regular ongoing updates of research studies.Assist in the development, review, and compliance of research protocols including but not limited to testing methodologies, statistical analysis, budget, ethical approvals, etc.Interface and collaborate with various departments and outside vendors to accomplish assigned tasks, including product design, product manufacturing, and design of applicable research studies on new products. Collaborate in the design and implementation of new methodologies, materials, and/or processes to bring concepts to market.Assist in meeting requirements of European Medical Device Regulations (EU MDR) and US Food and Drug Administration (FDA).Establish and maintain relationships with key customers, Universities, Government facilities, and private practices completing company-funded research.Frequently use software, such as SOLIDWORKS, MS Office, Adobe Acrobat, BarTender Designer, etc., to complete tasks.

Responsible for my research project on cardiac fibrosisFacilitated projects of post-docs by helping with their experiments Analysis of RNA and protein using various laboratory techniques

Worked with team members on designing a continuous passive motion device to aid in knee rehabilitation following total knee replacement surgery for UAB Hospital-Highlands. The device provides flexion and extension exercises for the post-surgery knee to prevent scar tissue development and other complications that might lead to a second surgery.

Mentor new International students