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Director, Clinical Data Management Operational Delivery

Takeda
USA - MA - Virtual, United States, United StatesRemotefull_timeVerifiedPosted 9 Jul 2026
💰 $278,080/yr($177,000/yr$278,080/yr)

About the role

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 and Terms of Use.  I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

Lead global implementation and adoption of new/enhanced Clinical Data Management (CDM) processes, ways of working, and technology (e.g., CFDR), while providing enterprise-level oversight of data management (DM) delivery, study timelines standardization, and inspection readiness across assigned assets/TAUs/portfolios.

 

  • The Director will be expected to lead implementation of new and enhanced processes, new ways of working and technology implementation projects (e.g., CFDR) within clinical data management (CDM), including:
    • Lead oversight and partner across CDSO and CDOS to ensure roll out. 
    • Identify risks and work with CDM LT and other Cross Function leaders to mitigate.
    • Coordinate with CDM LT to set initiative priorities.
    • Partner with Global Development Compliance (GDC) to implement and monitor rollout of new processes, tech, and ways of working.
  • Champions harmonization, change management and user adoption efforts across regions, TAUs and service providers.
  • Serve as Functional Process Owner and Expert (FPE) in Takeda’s continuous improvement framework:
    • Partner with process Business Process Owner (BPO), GDC, and BSO to ensure controlled and business-controlled process documents are complete, meet regulatory compliance (as applicable), and are optimized for end user needs
  • Lead champion/SME network (e.g., CFDR) to embed process and tech knowledge & proficiency in CDM functional members.
  • Lead and/or participate in process excellent and/or initiatives through operational implementation.
  • Partner across TAUs and roles to ensure consistent approach and implementation of process and ways of working.
  • Serve as lead CDM standards governance representative
  • Serve as lead CDM stakeholder and partner with BSO to ensure technology aligns with CDM roadmap,
  • The Director is responsible for effective leadership of setting up framework for tracking project timeline deliverables at an enterprise level for DM activities globally within and across a key asset, franchise/portfolio and/or therapeutic area(s).
  • Provides enterprise view of study timelines and status across the study lifecycle for DM end to end tasks from start-up through database lock at the TAU, program(s), and/or portfolio level.
  • Develop and maintain FTE and/or FSP Resourcing model and algorithm in alignment with CDM TAU LT and ensure consistent implementation across TAU according to the CDM vision
  • Drives significant levels of business change, within CDM and across the broader organization to ensure the successful execution of the CDM strategy and operating models.
  • Provides DM expertise in support of CDM operating model for TAU, program(s), and/or portfolio level.
  • Develop and maintain CFDR stakeholder management across SET roles to support operational excellence and escalation activities
  • Provide expert functional support guidance in audit readiness

 

Functional Service Provider (FSP) :

  • The Director may have direct line management responsibilities and/or supervisory responsibility for global FSPs.
  • Responsible for oversight of FSP resource allocation and DM strategic vendor partnerships to effectively deliver on internal and/or outsourced projects.

In-Direct line management:

  • Relationship manager, establishing and maintaining productive partnerships within Clinical Data Management (CDM), functional leaders across R&D, and third-party service providers.
  • Champions C

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Company

Takeda

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