Specialist I, Data Science

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:

​​​​​Join a growing oncology-focused organization where clinical data integrity directly supports innovative cancer therapies.

This role provides hands-on exposure to the full clinical trial lifecycle and offers development opportunities within Clinical Data Management and Data Science.​​​​

 

Position Summary:

​​​​​​​Specialist I, Data Science in Data Management department assists with the coordination and management of Taiho Oncology Inc., (TOI) clinical data management (CDM) activities performed by internal or various CRO teams for assigned clinical programs.

Responsibilities include assistance in study EDC set-up and testing, data review activities, as well as other data management tasks specified by Lead Clinical Data Managers.​​​​​​

 

Performance Objectives:


* Assistance in managing study conduct by providing relevant CDM input. 


* Work as hands-on clinical data specialist to support assigned programs by reviewing and contributing to CRF design, authoring/reviewing CRF completion guidelines, reconciling AE/SAE and other external data, reviewing clinical data as specified in the data review plan. 


* Collaborate closely with other functions within Data Science, Clinical Development and Clinical Operations during the data review and data issue resolution process.​​ 

 

Education/Certification Requirements:


* ​​​​​​Bachelor's degree in life sciences/relevant studies or equivalent or relevant working experience in lieu of a degree required​. Relevant internship or exposure to clinical trials a plus.​​​​ 

 

Knowledge, Skills, and Abilities:


* Basic knowledge of oncology research standards and best practice in data collection methodology and operational approaches preferred. 


* Understanding of ICH-GCP principles and regulatory expectations relevant to clinical data managemen...