Takeda Pharmaceuticals

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: This role...

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 Title: Associate Director, Clinical PV & Medical Quality, CPMQ Global Regions Location: US Remote About the role: As an Associate Director, Clinical PV & Medical Quality, CPMQ Global Regions, you will provide oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities in the commercial business units and affiliates. You will drive a fit-for-use global Quality framework that elevates the capabilities in the business units and the affiliate and enables them to...

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: This...

Associate Director, Clinical PV & Medical Quality, CPMQ Global Regions As an Associate Director, Clinical PV & Medical Quality, CPMQ Global Regions, you will provide oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities in the commercial business units and affiliates. You will drive 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. You will also establish and maintain relationships with key stakeholders outside R&D such as the commercial Business Units, affiliates. Global Medical, Commercial Quality, etc., supporting post-authorization strategies through thought partnership and linking R&D SMEs and experts, as needed. Provide expertise clinical research and pharmacovigilance regulations and compliance...

Associate Director, Medical Review The Associate Director, Medical Review, will serve as a functional expert in the area of Medical Review for their assigned region and products and ensure alignment and integration of process and technology efficiencies in medical review activities across diseases areas for Global Medical Affairs Oncology (GMAO). The individual in this role must excel in providing advanced medical and scientific review of commerical and medical affairs materials (promotional and non promotional materials) to support the non-promotional and promotional review processes. The Individual in this role will be responsible for performing timely, accurate and detailed scientific/medical review of non-promotional and promotional materials for the US and Global market in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs. He/she ensures Takeda non-promotional/ promotional materials convey accurate, correct...

Medical Affairs Scientific Training Manager OBJECTIVES/PURPOSE Responsible for identification of learning needs, development and execution of strategic, tailored training plans and packages, and measurement of training success for Medical Affairs Scientific Training plans within GMAO, which includes ongoing needs assessments, developing and updating training programs, and establishing reinforcement training, including booster and focal training, to drive continual enhancement of GMAO scientific knowledge of Takeda Oncology marketed and pipeline products, relevant disease states, and competitor data Ensure strategic collaboration with regions and countries to better understand training needs and deliver programs that meet these needs Work with and oversee vendors to help support training initiatives. Serve as a subject-matter expert and consultant to the regions and countries within GMA Liaise with members of the GMAO team and key cross-functional stakeholders, and be...