Senior Research Scientist at Oracle Risk Management Services

, , United States -

Full Time

Start Date

Immediate

Expiry Date

23 May, 26

Salary

158200.0

Posted On

22 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Health Outcomes Research, Real World Evidence, Tobacco Harm Reduction, Regulatory Studies, FDA CTP Submissions, Research Design, Data Analysis, Reporting, Behavioral Research, Regulatory Strategy, Cross-functional Collaboration, Scientific Rigor, Writing, Communication, Strategic Thinking

Industry

IT Services and IT Consulting

Description

Oracle Life Sciences is seeking a qualified health outcomes researcher with a Master’s or PhD to join our Real World Evidence Tobacco Harm Reduction team. In this role you will have the opportunity to lead the design, analysis, and reporting of regulatory studies (e.g., studies which need to meet the scientific rigor for FDA CTP submissions) and provide research consultation to both internal and external clients. This role requires a strategic thinker with strong research, writing, and communication skills. Oracle Life Sciences is looking for a strategic leader responsible for designing, executing, and interpreting behavioral research to support regulatory submissions, including PMTAs. The ideal candidate brings deep expertise in behavioral science, regulatory strategy, and cross-functional collaboration to ensure all data meets FDA requirements. Only Oracle brings together the data, infrastructure, applications, and expertise to power everything from industry innovations to life-saving care. And with AI embedded across our products and services, we help customers turn that promise into a better future for all. Discover your potential at a company leading the way in AI and cloud solutions that impact billions of lives. True innovation starts when everyone is empowered to contribute. That’s why we’re committed to growing a workforce that promotes opportunities for all with competitive benefits that support our people with flexible medical, life insurance, and retirement options. We also encourage employees to give back to their communities through our volunteer programs. We’re committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing accommodation-request_mb@oracle.com or by calling 1-888-404-2494 in the United States. Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans’ status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

This role involves leading the design, analysis, and reporting of regulatory studies, such as those required for FDA CTP submissions, while providing research consultation to internal and external clients. The scientist will be responsible for designing, executing, and interpreting behavioral research to support regulatory submissions, including PMTAs.