Takeda Pharmaceuticals Jobs & Careers - Remote Work From Home & Flexible
About Takeda Pharmaceuticals
Researched & Written by Carol Cochran on the FlexJobs Team
With a heritage dating back to 19th-century Japan, Takeda Pharmaceuticals has been in operation for more than two centuries, and its North American division was established in the United States in 1999 after being approved by the FDA. Headquartered in Tokyo, Japan, and present in 70 countries and regions across the globe, Takeda is now one of the world's top biopharmaceutical companies, specializing in a broad range of healthcare-related research and development.
武田制药致力于提供high-quality products that benefit individual wellness by developing innovative medicinal solutions. This mission drives the company's research and development of prescription drugs, marks its growth and success, and promotes its commitment to social responsibility. Takeda's work includes studies on diabetes, cardiovascular disease, central nervous system disorders, gastroenterology, bone and joint disorders, chronic kidney disease, gynecological disorders, and infectious diseases. Furthermore, the company is committed to environmental initiatives, such as reducing its carbon footprint and building a sustainable future, for which it has earned Gold LEED and Energy Star certification.
As an employer, Takeda Pharmaceuticals fosters a culture of compliance based on exercising integrity in decision-making and action-taking. The company is devoted to diversity and inclusion in its hiring practices, which Takeda considers a fundamental factor in its ability to serve unique patients, customers, and communities and reach its highest potential. The company also offers employee-based programs, including philanthropic efforts such as matching-gift programs and volunteer awards. In the past, Takeda Pharmaceuticals has offered part-time and full-time, remote jobs.
Visit Takeda Pharmaceuticals' websiteTakeda Pharmaceuticals on FlexJobs
Flexibility Offered
* Based on all jobs posted on FlexJobs
Karin K from Burrbank, CA—Hired at Takeda Pharmaceuticals as Webinar Producer
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For Research: Past Remote and Flexible Jobs at Takeda Pharmaceuticals
We include these past jobs as a way for you to explore what kinds of remote and flexible jobs Takeda Pharmaceuticals has hired for in the past and might be likely to hire for again in the future.
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30+ days ago当我们成功的人力资源解决方案专家,雇工e Lifecycle, you will provide back-office support services with a high degree of customer satisfaction, expertise, and timeliness. This includes evaluating the issue, quickly interpreting the situation...
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30+ days agoResponsible for the development, maintenance, and implementation of Company Core Data Sheets (CCDS) in line with international standards and guidelines. Provide strategic and tactical labeling expertise to teams while ensuring compliance with...
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30+ days agoExecute build and management, including all maintenance activities, of global site study budgets using industry tools and fair market value strategies. Execute study forecasting of global study site budgets, including reporting and oversight through...
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30+ days agoPosting of purchase invoices in accordance with the accounting standards. Monitoring payment deadlines and controlling the execution of payments. Replying to internal and external queries within agreed SLAs. Performing internal controls. Effective...
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30+ days agoYou will lead the execution of the transition of base data and emissions estimations from generic to supplier-specific emission factors. 5+ years relevant experience in Scope 3 accounting and LCA application in a corporate or consulting environment.
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30+ days agoWorking across therapeutic areas to provide expert support as needed the Principal Medical Writer formulates the writing strategy for key clinical and regulatory documents and regulatory submissions; guides medical writing document preparation...
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30+ days agoPlans and manages detailed publishing timelines; provides reporting on publishing status to key stakeholders. Proactively escalates publishing concerns, risks and issues that may delay/impact the submission and presents risk mitigation for publishing...
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30+ days agoDrive hands-on economic assessments for oncology medicines at all stages of development, using HE models and materials including systematic literature reviews (SLRs), indirect treatment comparisons (ITCs), statistical analyses of trial and real-world...
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30+ days agoLead data management activities for in-house and outsourced studies, and managing staff responsible for performing those activities. Manage vendor oversight activities across global development programs. Represent data management function on the...
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30+ days agoGlobal lead for regulatory policy research, including case studies, data-driven policy support, regulatory data analysis, visualization, and interpretation, public dataset identification and characterization, and hypothesis testing.
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30+ days agoAs a principal medical writer working on the medical writing team, you will be empowered to formulate the writing strategy for key clinical and regulatory documents and regulatory submissions. Formulate writing approach, develops timelines...
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30+ days agoProvide strategic quality oversight activities to PV business partners and suppliers that promotes operational and compliance excellence, quality risk management and knowledge management. Oversee and ensure compliant execution of the BPSQA audit program.
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30+ days agoResponsible for leading data management activities for in-house and outsourced studies; may manage staff responsible for performing those activities. Responsible for vendor oversight activities across global development programs. Represents data...
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30+ days agoLead or support training initiatives within the group and support maintenance of a balanced workload among nonclinical writers. Analyze, interpret and distill nonclinical data to independently manage a variety of projects of diverse scope...
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30+ days agoAs a Principal Medical Writer working on the Medical Writing team, you will be empowered to formulate the writing strategy for key clinical and regulatory documents and regulatory submissions; guide medical writing document preparation coordination...
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30+ days agoCreate and implement strategic communications plans to raise awareness and enhance reputation of R&D in Japan. Collaborate and coordinate with broader R&D Communications team to localize and disseminate global campaigns in Japan. Engage with Japan R&D...
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30+ days agoDrive the Hemophilia portfolio through management of branded and unbranded initiatives to support demonstrating payer coverage, health economic value, and comparative clinical efficacy, in support of driving formulary access and product selection.
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30+ days agoProvide support for critical day-to-day clinical study activities, in accordance with established protocols under the general supervision of the CTA Manager. Provide oversight of deliverables and milestones and/or lead CTA team during regulatory...
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30+ days agoLeads the creation and development of detailed analysis and forecast projections for all brands relating to pricing, rebates, and charge backs, which are incorporated into US BU P&L, directly affecting the organization's overall financial performance.
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30+ days agoSupport GCO LT Leader with communicating and championing their leadership vision, mission, and objectives. Serve as a positive and visible role model for change - actively engages their assigned leadership team to build sponsorship of key initiatives.
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30+ days agoWork closely with regulatory project managers to lead the production of high quality submission assemblies utilizing submission-ready documents that adhere to internal and external electronic submission guidelines. Ensure submission assemblies meet...
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30+ days agoRepresent pharmacovigilance department in cross-functional teams or committees and external environments at a global and regional level as required. In depth knowledge and understanding of designated products/studies. The attainment of advanced...
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30+ days agoProvides leadership to regional aggregate reporting team including training, mentoring, development, and appraisals. Assists in management of departmental budgets. Ensures aggregate reporting processes and procedures are complete and compliant.
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30+ days agoDesign, check for quality, and manage the distribution of monthly incentive compensation reports to the field and internal management. 3+ years of relevant experience in field sales incentive compensation administration and design.
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30+ days agoResponsible for developing the strategy for Strategic Partnerships with payer accounts & key customers. Develop/implement a vision & roadmap for the Managed Markets Access Analytics team. Facilitate the integrated strategy development & organizational...
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