Takeda

Associate Director, Scientific Training Lead, Global Medical Affairs Oncology Join to apply for the Associate Director, Scientific Training Lead, Global Medical Affairs Oncology role at Takeda . Base Pay Range $168,700.00 – $265,100.00 per year Job Description About the Role As a member of Takeda Oncology, your work will contribute to our bold, inspiring vision to cure cancer. Here, you will build a career grounded in purpose and be empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to the Head of Medical Excellence & Scientific Training and focus on developing, delivering, and measuring scientific training aligned with Takeda’s therapeutic goals. Responsibilities 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. This includes ongoing needs...

Overview Regional Account Medical Lead (Associate Director) at Takeda. The role involves working with Account Management (AM) and serving as the first-line Takeda medical point of contact for key accounts. You will develop medical strategies and tactics through a deep understanding of key accounts to support mutually beneficial partnerships. You will lead cross-functional efforts to deliver a partnership approach to pull-through medical strategies and tactics within key accounts. As part of the US Medical team, you will report to the Regional Director, Account Medical Lead Team. This is a field-based role and covers IL, KY, WI, KS, NE, MA, NJ, NY, RI, ME, NH, and VT (must reside in territory). The preferred incumbent locations are Boston, MA, New York City, New Jersey or Chicago, IL. Base pay range $168,700.00/yr - $265,100.00/yr By clicking the 'Apply' button, I understand that my employment application process with Takeda will commence and that the information I provide in my...

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 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. How will...

A leading global biopharmaceutical company is seeking a new team member to enhance training within its Oncology division. This role involves developing tailored training programs, collaborating with cross-functional teams, and ensuring compliance within medical affairs. Candidates must have a doctoral degree in a scientific discipline and significant experience in medical affairs or related fields. This position offers a hybrid working environment in Boston, MA, with a competitive salary range of $168,700 to $265,100. #J-18808-Ljbffr