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Facilitates and develops the relationship with the medical/scientific community by communicating product related information to investigators and institutions. Provides information on research developments and new concepts in medical treatment, giving perspective to field activities associated with growing existing products and bringing new products to market.
US
Taiho Oncology, Inc. works urgently to discover and develop innovative cancer treatments. As cancer evolves, we evolve with it—bringing novel technology to cornerstone chemotherapies, while at the same time optimizing new targeted agents. Advanced technology, dedicated investigators, and incomparable facilities—these vast resources empower us to redefine the way the world treats cancer. It’s our work; it’s our passion; it’s our legacy.  This position is responsible for driving sales for the launches of oncologic medications. The OAM reports to the Regional Business Director
US-NJ-Princeton
Taiho Oncology, Inc. works urgently to discover and develop innovative cancer treatments. As cancer evolves, we evolve with it—bringing novel technology to cornerstone chemotherapies, while at the same time optimizing new targeted agents. Advanced technology, dedicated investigators, and incomparable facilities—these vast resources empower us to redefine the way the world treats cancer. It’s our work; it’s our passion; it’s our legacy.   Manager, Financial Planning & Analysis is responsible for managing the Taiho Oncology, Inc.’s (TOI’s) and Taiho Pharma Europe Ltd.’s (TPEL’s) overall budget and forecasting process, providing the Sr. Director of Finance and the VP Finance with timely and accurate data and analysis. In addition, this job is required to perform monthly cash flow projection and analysis.
US-NJ-Princeton
Position Summary:            Under the leadership of the Director/Senior Director, CMC Regulatory Affairs the incumbent manages the global regulatory CMC activities except Asia for all Taiho Oncology Inc., (TOI) projects, provides strategic CMC regulatory guidance during drug development, approval, post approval, and commercialization, in coordination with internal staff and external consultants/contractors. Manages the development and preparation of high quality CMC sections of the regulatory submissions including NDA's, MAA's, INDs, CTAs, DMFs, ASMFs, etc., and ensures that they conform to current GMP and global regulatory requirements. The incumbent interacts with regulatory authorities during the drug development and approval processes following an agreed upon plan.
US
Facilitates and develops the relationship with the medical/scientific community by communicating product related information to investigators and institutions. Provides information on research developments and new concepts in medical treatment, giving perspective to field activities associated with growing existing products and bringing new products to market.
US-NJ-Princeton
Reporting to the Vice President, Medical Affairs and Pharmacovigilance, the Director, Medical Affairs is responsible for providing medical support to the Company’s product development strategy and post marketing commitments, while supporting Medical Affairs strategy related to the Investigator Sponsored Trials (IST) program. This individual will interface with physicians, clinical investigators, regulatory agencies and internal departments.  The Director, Medical Affairs must possess an in depth knowledge of oncology products, agents in the pipeline, and all associated disease areas. This position will provide leadership within Medical Affairs and may represent the department at key internal and external meetings.  This position will include providing input on marketing programs and representing the company at scientific, clinical and business development meetings.
US-NJ-Princeton
This position is for a Manager, IT Applications to manage Taiho’s business applications providing daily support, release planning, oversight, and support. The successful candidate will lead the implementation of application and enhancement projects from planning through deployment and support. Manager is responsible for developing solutions to enhance the system, ensuring that support processes are managed properly under the direction of the supervisor. The role will also function as a liaison between IT and the Business Client, and act as the go-to person that represents the application team support. The initial focus will be in the area of R&D systems.