Sr. 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: 3-days per week on-site

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 design, execution and reporting of current and future clinical oncology trials ranging from phase 1 – 3.

 

Performance Objectives:


* Assumes the medical leadership on clinical trials for Taiho Oncology, Inc.

(TOI) in the USA and Europe.


* This position serves as a responsible medical monitor or a Lead medical monitor for various clinical phase 1 - 3 trials, as needed.


* Uses medical/scientific expertise to create or support the creation of relevant clinical   documents of high quality such as study concepts, study protocols and reports, investigator   brochures, NDA/MAA registration documents and publications.


* Reviews and signs off on clinical documents related to clinical studies as outlined by the   manager.


* Builds and maintains effective relationships with clinical key opinion leaders in various   different areas of disease in which Taiho is developing drugs.


* Will collaborate with all department heads within TOI (Head of Clinical Research and Head of Clinical Operations) to establish operational plans and timelines for respective studies within each of the development programs for review by the SVP Clinical Development or the Chief Medical Officer. 


* Keeps SVP Clinical Development or the Chief Medical Officer current on status of clinical trials and provides ongoing risk assessments for the study conduct and operational risks. 


* Co-responsible with SVP Clinical Development, Project Management, ...