11 associate director global rwe jobs found in Boston

Associate Director, Clinical PV & Medical Quality, CPMQ Global Regions Join to apply for the Associate Director, Clinical PV & Medical Quality, CPMQ Global Regions role at Takeda . Base pay range: $153,600.00/yr - $241,340.00/yr. U.S. based employees may be eligible for short‑term and/or long‑term incentives and a variety of benefits including medical, dental, vision, 401(k), disability, life insurance, tuition reimbursement, paid volunteer time off, holidays, well‑being benefits, up to 80 hours sick time and 120 hours paid vacation for new hires. Salary will reflect qualifications, experience, education, certifications, location, and applicable wage requirements. 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...

Associate Director, US HCP Marketing, Medical Education How will your role help us transform hope into reality? As Associate Director, US HCP Marketing, Medical Education Lead, you will play a pivotal role in transforming the landscape of systemic mastocytosis (SM) care in the United States. You will lead the development and execution of strategic, data-driven education and engagement initiatives that empower healthcare professionals (HCPs) across multiple specialties to recognize, diagnose, and treat SM, including Indolent Systemic Mastocytosis (ISM) and Advanced Systemic Mastocytosis (AdvSM), with AYVAKIT (avapritinib). By championing innovative approaches to HCP engagement and leveraging insights from real-world experience and emerging data, you will address the significant challenge of underdiagnosis and help improve patient outcomes across the full spectrum of SM. In this role, you will shape educational content, peer-to-peer programs, advisory boards, congress...

Associate Director Of Strategic Planning & Execution For Us Medical Affairs Are you ready to make a significant impact in the world of rare diseases? As the Associate Director of Strategic Planning & Execution for US Medical Affairs, you will drive strategic initiatives and collaborate with Therapeutic Area (TA) Leadership teams to align projects with our overarching goals. Your role will involve analyzing, resolving, and communicating key strategic programs, enabling informed decision-making that contributes to our success. With your project management expertise, you'll ensure projects are delivered on time, within scope, and on budget. Responsibilities Strategic Partnership: Develop annual enterprise strategy for assigned TA and/or Function and ensure effective, efficient, and equitable delivery of key strategic programs and operational activities Oversight of business progress against performance targets through outcomes and metrics tracking/reporting Highlight...

Associate Director, Scientific Communications Lead, Solid Tumors As a member of Takeda Oncology, your work will contribute to our bold, inspiring vision: We aspire to cure cancer. Here, you'll 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 Scientific Communications Group Lead, Solid Tumors. As a subject matter expert on scientific publications best practices and the development of scientific communications strategy and deliverables, the Associate Director, Scientific Communications Lead, Solid Tumors proactively defines and drives the publication and scientific communication strategic plan and deliverables for the assigned oncology assets based on medical strategies, transparency requirements, and data availability. This position requires a strong scientific and analytical background, preferably in life sciences, and excellent project management skills. The Associate Director,...

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 About the role: As a member of Takeda Oncology, your work will contribute to our bold, inspiring vision: We aspire to cure cancer. Here, you'll 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 Scientific Communications Group Lead, Hematology. As a subject matter expert on scientific publications best practices and the development of scientific communications strategy and deliverables, the Associate Director, Scientific...

Associate Director Medical Writing (Hybrid) page is loaded## Associate Director Medical Writing (Hybrid)locations: Boston, MAtime type: Full timeposted on: Posted Yesterdayjob requisition id: REQ-27415**Job Description****General Summary:**The Associate Director, Medical Writing Science manages the overall operations of a team or major project and implements this through effective leadership. This role provides guidance and leadership for document development for regulatory filings and coordinates the clinical sections of more complex regulatory submissions, including organization, content, and resource requirements. This role applies advanced technical expertise and develops solutions to complex problems, fosters interdisciplinary understanding, and integrates Medical Writing Science department activities with those of other departments.This is a hybrid role which allows for 2 days per week remote work and 3 days per week in the Boston Fan Pier office. We offer a full...

Associate Director Strategic Business Planning and Execution, US Medical Affairs Alexion Pharmaceuticals, Inc. is seeking an experienced Associate Director of Strategic Planning & Execution for US Medical Affairs to drive strategic initiatives and collaborate with Therapeutic Area (TA) Leadership teams. As the Associate Director , you will analyze, resolve, and communicate key strategic programs, ensuring projects are delivered on time, within scope, and on budget. Responsibilities Strategic Partnership Develop annual enterprise strategy for assigned TA and/or Function and ensure effective, efficient, and equitable delivery of key strategic programs and operational activities. Oversee business progress against performance targets through outcomes and metrics tracking/reporting. Highlight and communicate US Medical impact and effectiveness throughout all levels of the organization. Proactively apply business acumen to ensure business continuity and identify future...

Are you ready to make a significant impact in the world of rare diseases? As the Associate Director of Strategic Planning & Execution for US Medical Affairs , you will drive strategic initiatives and collaborate with Therapeutic Area (TA) Leadership teams to align projects with our overarching goals. Your role will involve analyzing, resolving, and communicating key strategic programs, enabling informed decision‑making that contributes to our success. With your project management expertise, you'll ensure projects are delivered on time, within scope, and on budget. Responsibilities Strategic Partnership Develop annual enterprise strategy for assigned TA and/or Function and ensure effective, efficient, and equitable delivery of key strategic programs and operational activities Oversight of business progress against performance targets through outcomes and metrics tracking/reporting Highlight and communicate US Medical impact and effectiveness throughout all levels of the...

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 Title:** Principal Medical Writer Associate Director**Location**: USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable for attending occasional team meetings**About the Job**Global Medical writing and Document management serves to generate timely, high quality, cost effective and regulatory compliant documents. Our mission is to synergize and harness evolving technologies pushing the edge of regulatory writing.**Main Responsibilities:****Document Development*** Create high-quality regulatory-compliant clinical documents supporting product life cycle* Ensure timely delivery while maintaining compliance with standards**Innovation*** Lead implementation of new digital technologies and AI solutions* Drive process improvements for efficiency gains**Regulatory Expertise*** Prepare registration dossiers and Health Authority responses* Monitor and implement regulatory documentation requirements**Project Management*** Lead cross-functional initiatives...