Director, External Research

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: 


* Utilizing scientific expertise in hematology and oncology, the Director, External Research will enjoy collaborating with Medical Affairs Product Leads on development of the areas of interest, execution of research collaborations and continued monitoring and reporting on key milestones.

This position will mentor, develop and have oversight of a direct report responsible for day-to-day operations for the research program including Investigator Initiated Trials/Collaborative Research (IITs/CR) and Independent Medical Education Programs.

Position Summary: 


* The Director is accountable for the External Research Program (IITs/CRs) for the Taiho Oncology Inc.

(TOI) portfolio in the US and Europe.

This role requires scientific expertise and experience in development and leads the IIT and collaborative program with continuous monitoring and reporting of key milestones.

In addition to interactions with Medical Affairs Product Leads, this role will engage with Medical Field team, global Sponsor-Investigators and lead the process for assessment of the IITs/Collaborative Research proposals, approvals, and communications.

Oversight of monitoring of the key milestones and appropriate action, and reporting will be essential for this role.

The candidate must ensure that Medical Affairs adheres to all applicable SOPs, laws, and regulations for compliance and quality.

Performance Objectives: 


* Leads, develops, and continuously improves the IITs/Collaborative Research Program for the TOI portfolio in the US and Europe, including scientific/clinical assessment of proposals, project management, and interface with Sponsor-Investigators.


* Monitoring and tracking of key milestones, analysis of scientific data from IITs/Collaborative studies and summarizes information for relevant reporting and communications, contributions to Life Cycle Management Plan, and reports to Medical Affairs Leadership....