Specialist I, Data Management

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:

​​​​​​​The Specialist I, Data Management 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 management. 
• Foundational understanding of data review, discrepancy management, and data reconciliation concepts. 
• Ability to use highly technical and AI-based data operations tools. Actual AI-related project experience is desirable. 
• Effective oral and written communication skills required. 
• Teamwork and interpersonal skills required. 
• Highly detail and quality oriented. 
• A positive attitude, flexibility and a proactive thought process.  
• Ability to review and present information effectively to internal and external functions. 
• Ability to define problems, collect data, establish facts, and draw valid conclusions.​ 

The pay range for this position at commencement of employment is expected to be between $73,950- $87,000 annually. This pay range is based on the market range for positions of this type. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including annual bonus/incentive comp plans, potential long term incentive plan, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if a candidate/employee receives an offer of employment. 

If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

#Location-Princeton,NJ #Location-Pleasanton, CA #LI-Hybrid

Equal Opportunity Employer Information: Taiho Oncology is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, sexual orientation, physical or mental disability, medical condition, veteran status, gender identity, genetic information, or any other characteristic protected by federal, state, or local law. Any applicant who, because of a disability, needs an accommodation or assistance in completing an application or at any time during the application process, please email People@taihooncology.com. Taiho Oncology also provides reasonable accommodations to employees with disabilities consistent with our obligations under the law. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment qualified applicants with arrest and conviction records.

The incumbent in this position may be required to perform other duties, as assigned.

Salary : $74 - $87