Idaho State Job Bank is hiring: Associate Director, Nonclinical Regulatory Writi

Associate Director, Nonclinical Regulatory Writing and Submission Support at Takeda Pharmaceuticals in Boise, Idaho, United States Job Description By clicking the 'Apply' button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Associate Director, Nonclinical Regulatory Writing and Submission Support, Gastrointestinal and Inflammation (GI2) and Neuroscience (NS) Products At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on three therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. Are you looking for a patient-focused, innovation-driven company that enables you to engage in meaningful work? Join us as an Associate Director - Nonclinical Regulatory Writer and Submission Support reporting to the Nonclinical Regulatory Writing and Submission Support, GI2 and NS Products Team lead, based in Cambridge, MA/Virtual. Here, you will be a vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing and Systems (NRWS) Department within Preclinical and Translational Sciences (PTS), you will be contributing to this science driven, collaborative and dynamic environment, bringing experience to add further value to the NRWS contribution to the PTS organization and to Takeda, with involvement in a variety of projects of diverse scope and complexity, reflecting the breadth of Takeda's portfolio, including Oncology (ONC), GI2, and NS. The NRWS team is a goal- and results-driven team, and we are strong believers in innovation and streamlined processes. How you will contribute: ACCOUNTABILITIES + Provides nonclinical regulatory writing expertise and mentorship to NRWS and Research and Development (R&D) staff members. + Involves in a variety of projects of diverse scope and complexity, across all developmental stages (pre-development through post-marketing) and Takeda's major therapeutic areas with focus on Gastrointestinal and Inflammation (GI2) and Neuroscience (NS) Products across Takeda's portfolio. + Applies advanced knowledge and experience to assess document requirements, develop writing strategy, compose dr To view full details and how to apply, please login or create a Job Seeker account