Assoc Dir, Clinical Pharmacovigilance and Medical Quality (CPMQ) Operations (Hybrid)
Takeda · Cambridge, Massachusetts, US
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my applic...
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. OBJECTIVES/PURPOSE: - Advance strategic quality leadership by embedding global standards across Clinical, Pharmacovigilance, and Medical Quality (CPMQ), ensuring regulatory alignment and operational excellence. - Drive innovation and transformation through organizational planning, digitalization, and capability building—enhancing systems, analytics, and process efficiency across CPMQ and R&D. - Strengthen quality oversight and risk management, leading compliance strategies, monitoring systems, and continuous improvement initiatives that mitigate systemic risks and foster resilience. - Serve as a strategic partner and change agent, shaping clinical trial delivery transformations, guiding GCP strategy, and aligning quality initiatives with enterprise priorities and a culture of learning. ACCOUNTABILITIES: - Identify and lead innovative tran...