Executive Medical Director, Clinical Development

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 Oncology, 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 lead global clinical trials and experience multiple facets of Clinical Development in a dynamic, supportive, collaborative, and global cross-functional environment.

Position Summary: 


* ​​This position has direct responsibility for leading global development program(s), including strategy, design, oversight, and analysis of Phase 1-4 oncology clinical trials.

This position will be the medical point of contact for all aspects of studies within the program(s) and accountable for program deliverables.

Performance Objectives: 


* Medical global lead for development program(s)


* Provide oversight for global Phase I-III and “ancillary” trials as Lead medical monitor for global development program(s)


* Use medical/scientific expertise and strategic thinking to develop clinical development plans (incl.

study design and companion diagnostics)


* Take accountability for strategy and deliverables of assigned global development program(s)


* Medical point of contact for all clinical questions related to the development program.


* Perform data review supported by Clinical Research Scientist(s) (CRS), participate in protocol deviation meeting that will occur monthly or as needed.


* Create or support the creation of relevant clinical documents of high quality, such as study protocol protocol(s), investigator brochure (IB), informed consent forms (ICF), case report forms (CRF), Clinical study report (CSR), NDA/MAA registration documents, and scientific publications.


* Analyze and interpret outcome of clinical studies within the global development program(s)


* Answer medical questions raised by Regulatory Agencies (RA) and Institutional Review Boards/ Ethic...