- Takeda Pharmaceuticals (Providence, RI)
- …of my knowledge. **Job Description** **_Objective / Purpose:_** + Member of the Nonclinical Regulatory Writing and Submissions (NRWS) leadership who drives ... across all programs and meet corporate goals by managing nonclinical regulatory writing activities. +.../compliance deadlines and lead internal/external and scientific teams to regulatory submission aims. + Thorough understanding of… more
- Takeda Pharmaceuticals (Providence, RI)
- …(eg, biology, pharmacology, toxicology), with minimum of 8 years of experiencewith nonclinical regulatory writing within the pharmaceutical industryor ... by integrating automation and innovative practices into the technical and regulatory writing framework, streamlining processes and fostering an environment… more
- Sumitomo Pharma (Providence, RI)
- …authors, and prepares regulatory submissions and works closely with Regulatory Operations in the electronic submission + Assesses and communicates ... with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical , clinical and CMC documentation (eg nonclinical ...and the ability to contribute to the development and writing of a regulatory strategy document +… more