Our Mission: Otsuka-people creating new products for better health worldwide
Welcome to Otsuka
These are exciting times for all of us at Otsuka in the U.S. We not only have a rich portfolio of products making real differences in areas of unmet medical need, but we also have many investigational products at various stages of development. Our work in digital medicine promises to pioneer a new behavioral healthcare paradigm, and our commitment to patients persists in our transformative support programs.
Turning vision into reality requires passion, leadership, dedication, diversity of thought, collaboration, and perseverance. Otsuka-people have these qualities in abundance, and we support them by providing a dynamic work environment that encourages them to explore ideas, seize opportunities, and grow in meaningful ways. Our passionate leadership and unique culture, combined with access to continuing education, a unique workspace, and top-of-the-line 401(k) retirement savings plans with matching contributions, among other benefits, make Otsuka a truly different place to learn and grow.
For more information, visit www.otsuka-us.com.
To be a credible source of evidence based information that demonstrates the value of Otsuka products from the clinical, economic and humanistic standpoint and works in partnership with providers, payers and other key stakeholders to apply practical real-world solutions to improve patient outcomes
Key Job Responsibilities:
Participate and interact with opinion leaders, local practice leaders and other key stakeholders, including preparing moderators at national, regional and local conferences, advisory boards and other approved gatherings.
Gather scientific and competitive intelligence as well as customer insights during interactions with opinion and practice leaders or attendance of congresses and communicate to relevant Medical Affairs and Clinical Development personal.
Evaluate and assess potential investigational sites for participation in Otsuka-sponsored clinical studies as well as educate investigators about the study drug and pharmacovigilance procedures.
Preferred location is Houston, TX, but Austin or San Antonio are reasonable locations also.