Entrepreneurial Spirit, Rooted in Tradition. At Mitsubishi Tanabe Pharma Development America (MTDA), we can tout a storied reputation more than 300 years in the making. Our parent company, Mitsubishi Tanabe Pharma Corporation (MTPC), is a research-driven pharmaceutical company with global reach – and one of Japan’s oldest and most respected companies.
Relatively new to the U.S. market, the innovative compounds of the Mitsubishi Tanabe Pharma Group have already enjoyed commercial success under the brand labels of our U.S. partners. In this next phase of development, we plan to bring exciting new compounds to market under our own MT Pharma America label. We’re currently building a new commercial organization and expanding our other functions to support this strategy.
The Drug Safety Specialist is responsible for completing all aspects of individual case safety report (ICSR) processing and reporting for assigned investigational and marketed products, while also assisting management in implementing departmental strategy. The Drug Safety Specialist supports and participates in drug safety assessment and management. The Drug Safety Specialist serves as a liaison to external service providers (i.e. clinical research organizations), investigational sites, and company personnel for safety-related issues, working in close collaboration with colleagues from Clinical Research, Data Science, Regulatory and Quality Assurance.
This is a 8 month contract position