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Sr. Clinical Trials Associate Manager
Lexington, Massachusetts- Job Level: Senior
- Travel: Minimal
At Takeda, we exist to create better health for people and a brighter future for the world. While we continually evolve science and technology, our ambition remains steadfast — we move science forward so we can transform more lives. The Global Development Organization (GDO) maintains a laser focus on Study Management and Site Engagement, Clinical Trial Innovation, Clinical Supply Chain and Patient Safety to ensure absolute quality and enable the predictable delivery of our innovative pipeline.
Through its collaborative process, the GDO team leverages data, digital and analytics to improve speed, quality, performance and predictability within every area of clinical development. We’re building a platform to visualize operational data and enable predictive analytics, while leveraging digital technologies to support clinical supply chain and patient safety. GDO also partners with external organizations and leading academic institutions, such as MIT, to spark innovation in AI and Machine Learning focused on better patient outcomes.
At the heart of GDO are our people: we are committed to building a more diverse, equitable and inclusive culture not only within our own walls and our communities, but also across our clinical trials. It is our passion for people that transforms our work into meaningful action. Come join a team that has earned trust for more than two centuries and advances transformative therapies with honesty, integrity and fairness.
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Job Description
Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc.for the following job opportunity:
JOB LOCATION:Lexington, MA
POSITION: Sr. Clinical Trials Associate Manager
POSITION DESCRIPTION: Takeda Development Center Americas, Inc. is seeking a Sr. Clinical Trials Associate Manager with the following duties:Manage and oversee clinical trial activities and ensure optimal use of resources and skillsets to deliver effective clinical trial support; Responsible for line management, ensuring appropriate training and oversightto ensure consistent and high-quality trial support across programs; Ensure resources are aligned to resourcing strategies and business critical goals and milestones, in collaboration with CTA Management team and Clinical Operations Lead(s); Act as subject matter expert to support complex activities such as process development, complex program support or department and/or business critical initiatives and deliverables. Up to 10% domestic and international travel required; Up to 100% remote work allowed.
REQUIREMENTS: Bachelor’s degree in Public Health or related field plus 5 years of related experience. Prior experience must include: Utilize line management skills through various mentorship roles; Provide expertise on process development and departmental critical deliverables; Preparestrategies to support complex studies through critical thinking; Provide leadership to functional team and study teams for more complex studies.
Full time. $149,600.00 - $228,000.00per year. Competitive compensation and benefits.
Qualified applicants can apply athttps://jobs.takeda.com. Please reference job #R0145616. EOE
Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.
Locations
Lexington, MAWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeThe heart of our work
Shining a light on new perspectives
Our pipeline
Our internal research capabilities and external partnerships contribute to an R&D engine that has produced exciting new molecular entities (NMEs) across our core Therapeutic Areas. Check out our pipeline and see how we’ll continue delivering a steady stream of next-generation therapies.
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Responsibly translate science into highly innovative medicines and accelerate access to improve lives worldwide.
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