Research Enablement Lead, Director

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Join Takeda as a Research Enablement Lead, Director in our Cambridge office. We are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.
Please make sure you read the following details carefully before making any applications. The Research Enablement Lead, Director supports a specific drug discovery unit (DDUs) or platform group in the delivery of critical Research priorities, serving as the sub-functions de facto Chief of Staff. Reporting to the Head of Japan Enablement Leads, the Lead plays a crucial role in the strategic planning, execution, and optimization of functional projects. Accountabilities Partners closely with Drug Discovery Unit (DDU) and Platform senior leadership to coordinate and prioritize activities. Provides strategic and operational support to Research leaders, including change and project management. Supports DDU and Platform senior leadership in managing and allocating resources effectively. Proactively identifies areas for process improvement within functional operations. Facilitates collaboration and communication among different teams and stakeholders. Engages with internal and external stakeholders to understand and address needs in alignment with Research priorities. Ensures smooth cross-functional liaisons with critical functions. Facilitates navigation of organizational processes and procedures. Identifies potential risks and challenges that may impact functional operations. Identifies and develops programs to meet research staff training requirements. Fosters a culture of continuous improvement by implementing best practices. Additional Responsibilities Portfolio/Project Management Support for Early-Stage Small Molecule Projects Manage project timeline information Facilitate alignment across TVS, DDU, GC, GB, and S&O functions Support global communications
CRO Management Support for In Vitro Pharmacology Ensure IVP group operates efficiently and effectively Manage requests and routine assay information Oversee contractual information related to licenses for in vitro assays Support financial information management
Compound Logistics Optimization Support Coordinate with Import/Export, DMPK, Safety, and IT teams Contribute to building a cross-functional business framework
Lab Equipment Information Management Coordinate CAPEX-related activities Oversee information management for equipment maintenance contracts Manage contractual information for both hardware and software
Education & Competencies Expected 12+ years related experience in the pharmaceutical industry, with expertise in drug discovery and Takeda therapeutic areas. Exceptional leadership and communication skills. Excellent project management and organizational skills. Experience as a team member in small molecule drug discovery projects. Strong knowledge of drug discovery and development processes. Deep understanding of the small molecule drug discovery process. Strategic mindset and the ability to think critically and creatively. Strong knowledge of business operations planning, change management, analytics, and reporting. Advanced degree (Ph.D., M.D., or equivalent) in a scientific discipline preferred. Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
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Location:
Boston, MA
Job Type:
FullTime
Category:
Management And Consultancy

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