Associate Director, PV Medical Surveillance

Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers.

Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission.

Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust.

By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other.

Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients.

Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients.

It’s our work, our passion, and our legacy.

We invite you to join us.  

Hybrid  

Employee Value Proposition: 

At Taiho, the compassion we practice for our patients extends to our team, empowering and motivating them to do their best work for those who need it most.  This is an exciting opportunity to work for early to late-stage global clinical trials and post-marketing products.

You will contribute to the growth and exciting change happening at Taiho Pharmacovigilance and have greater opportunity to expose/contribute to the company’s portfolio.

With competitive compensation, comprehensive benefits, and a commitment to professional development, Taiho empowers you to thrive personally and professionally.

Join us in our mission to and be a part of the Taiho evolution to have your imprint based on your experience in our rapidly evolving organization.

Position Summary: 


* ​​The incumbent will be responsible for global medical surveillance for Taiho, marketed and/or investigational products assigned, including review and analysis of safety data from clinical trials and from post-marketing sources, providing medical expertise to assigned project teams, the identification and investigation of safety signals, management of benefit-risk profile for assigned products and review of aggregate reports.

Responsible for keeping upper management informed of safety issues.

This is a critical role to ensure safety of patients taking Taiho investigational and marketed products.

Performance Objectives:


* Demonstrates knowledge of safety, including any emerging safety concerns and risk/benefit profile for responsible compounds, as well as regulatory guidelines as they pertain to drug safety/pharmacovigilance.


* Responsible for Individual Case Safety Report (ICSR) review.

Ensures completeness and accuracy of safety information in individual case reports through assessment of seriousness, expectedness, and causality, coding, review of narrative summary and providing case comments; provide medical inq...