Associate Director, Clinical Research Scientist

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, we are dedicated to transforming the landscape of cancer treatment and improving patients' lives.

As an Associate Director, Clinical Research Scientist, you will play a pivotal role in our mission, leveraging your expertise to drive innovative clinical research and contribute to groundbreaking therapies.

We offer a collaborative and inclusive work environment where your ideas and contributions are valued.

Join us to advance your career, work with passionate and skilled professionals, and make a meaningful impact on the fight against cancer.

At Taiho Oncology, you will find purpose, growth, and the opportunity to be at the forefront of cancer research.

 

Position Summary:

The Associate Director, Clinical Research Scientist has responsibility assisting in design, execution and reporting of current and future clinical oncology trials ranging from phase 1 - 3.

Additionally, this role serves in assisting the responsible medical monitor or a Lead medical monitor for various clinical phase 1 - 3 trials, as needed.

 

Performance Objectives:


* Uses medical/scientific expertise to support the creation of relevant clinical documents of high quality such as study concepts, study protocols, amendments, study reports and investigator brochures.


* At the asset level, assists the medical lead in the preparations of the clinical content of regulatory submissions/documents (e.

g.

NDA, MAA, IND, CTA.

sNDA, DSUR, PIP, health authority/ethics committee responses, briefing packages).


* Works with the medical lead to prepare presentations (internal and external), abstracts, manuscripts.


* Inputs into the of ICF/reviews ICF.


* Works with data management on CRF design and completion guide.


* Partners with data management to develop data review plan for review of data and with medical lead for the medical monitoring plan.


* Reviews protocol deviations, patient eligibili...