Takeda Pharmaceuticals

Job Title 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. Job Description Objectives: Provides oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities in the commercial business units and affiliates. Contributes to and implements the engagement strategy among R&D, Business Units and affiliates and Quality to ensure a global framework and robust quality systems are in place for the transition of R&D pipeline to the commercial space. Drives a fit-for-use global Quality framework that elevates the capabilities in the business units and the affiliate and enables them to deliver their clinical research and pharmacovigilance-related regulated activities with high compliance and agility. Establish and maintain relationships with key...

Pharmacovigilance Scientist Principal responsibilities include: Supports the Global Safety Lead (GSL) for assigned oncology pharmaceutical/biological/drug-device combined products. Responsible for safety surveillance, signal detection and risk management activities. Supports cross-functional assessment of benefit-risk profile and communication of safety information for assigned compounds and products. Provides pharmacovigilance functional area expertise and support to project teams for assigned developmental and/or marketed products. Represent pharmacovigilance, both regionally and globally, as an authoritative and knowledgeable member of Global Program Teams (GPTs) and subteams, commensurate with position's seniority/experience. Coordinates all aspects of signal detection and safety surveillance and review activities, in collaboration with the GSL, for assigned product(s). Analyze and interpret safety data from various sources including non-clinical, clinical,...

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 (https://jobs.takeda.com/privacynotice) and Terms of Use (https://www.takeda.com/terms-and-conditions/) . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description OBJECTIVE: Principal responsibilities include: Supports the Global Safety Lead (GSL) for assigned oncology pharmaceutical / biological / drug-device combined products. Responsible for safety surveillance, signal detection and risk management activities. Supports cross-functional assessment of benefit-risk profile and communication of safety information for assigned compounds and products. Provides pharmacovigilance functional area expertise and support to project teams for assigned developmental and/or...

Job Description OBJECTIVES/PURPOSE: The Medical Communications Associate Director is a strategic partner of the US Medical Communications team responsible for supporting the development and execution of the medical communications strategy across the assigned therapeutic portfolio. Actively involved in the medical communications Scientific Communication Platform (SCP) and Integrated Communication Platform (ICP) development; content generation, which may include, but is not limited to, scientific slide decks, field medical tools, training materials, congress-related activities, websites/tools, and other medical programs. Supports execution of key medical communications tactics and activities, in an independent manner, closely coordinated with the Director US Medical Communications. The Medical Communications Associate Director is a member of the Scientific Communications Team reporting to the Director US Medical Communications for the assigned therapeutic area. SCOPE:...