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Takeda

Strategy & Operations Lead—Medical Trial Enablement & Early Pipeline

Location
Boston, MA (MA)
Posted
Posted today (employer shows the date only)
Source
Workday (employer's applicant tracking system)
Category
Operations/Patient Services
Industry
Pharma/Biotech
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Job Description

Join Takeda Oncology as a Strategy & Operations Lead- Medical Trial Enablement & Early Pipeline (Associate Director) out of our Cambridge, MA office. The S&O Lead for Medical Trial Enablement & Early Pipeline strengthens and scales Medical’s support for oncology clinical trials across the portfolio. Reporting to the GMAO Chief of Staff, the role leads the planning, coordination, implementation, and continuous assessment and improvement of the GMAO clinical trial enablement model by translating clinical development plans and study timelines into clear Medical requirements, integrated readiness plans, and coordinated execution. The S&O Lead partners with GMAO Medical, Global Development Operations, senior leaders, and Global, Regional, and Local Medical teams to enable proactive, consistent, and timely support for new and ongoing trials. This role involves change management, communication planning, and enhancing team collaboration to contribute to the overall success of Global Medical Affairs effectiveness and operations.

Accountabilities:

  • Lead strategic initiatives on behalf of the GMAO CMO and Chief of Staff that strengthen Medical’s contribution to clinical trial planning, start-up, execution, and acceleration across the oncology portfolio, ensuring clear responsibilities and coordinated execution across Global, Regional, and LOC Medical teams.
  • Lead integrated planning across GMAO clinical trial support activities, including milestones, decision points, dependencies, risks, deliverables, and measures of success.
  • Maintain a forward-looking view of trial milestones and Medical support needs. Partner with Regional and LOC Medical leaders to confirm owners, preparation requirements, and resource capacity, and escalate gaps before they affect execution.
  • Establish clear governance, roles, handoffs, escalation routes, and communication pathways for GMAO clinical trial support across Global, Regional, and Local Medical teams.
  • Ensure appropriate Medical representation in key feasibility, country and site planning, and study execution forums, with clear expectations for input and timely communication of decisions to relevant Medical teams.
  • Partner with Global Medical Leads to optimize meeting management and team effectiveness for GMA core and strategic teams for early pipeline program.
  • Track Medical recommendations, requests, and escalations through resolution, ensuring decisions, rationale, and next steps are communicated back to contributing teams.
  • Represent GMAO on digital innovation efforts to define and prioritize Medical requirements and enhance cross-functional impact on clinical trial execution.
  • Continuously assess workflows and processes with cross-functional partners; identify and prioritize improvement opportunities; implement changes that reduce complexity and strengthen execution; and monitor adoption, outcomes, and realized benefits to inform further refinement.
  • Develop executive-level updates and decision materials that provide transparent visibility to readiness, milestones, risks, dependencies, and required actions.

Dimensions and Aspects:

  • Communicates ideas and data clearly and persuasively, both verbally and in writing.
  • Builds credibility, trust, and confidence as an effective team member within and outside the company.
  • Distills complex concepts into clear, accessible, and actionable language.
  • Maintains high standards of excellence and thrives in a dynamic, cross-functional environment.
  • Leads complex, cross-functional projects from ideation through execution.
  • Manages multiple priorities with attention to detail and strong organizational discipline in a fast-paced environment.
  • Collaborates proactively with a solution-focused mindset.

Education, Behavioral Competencies, and Skills:

Required:

  • Bachelor’s degree required; advanced degree (MBA, MPH, PhD, etc.) preferred.
  • 5+ years of experience in medical affairs, clinical development, clinical operations, program management, or a related role within the pharmaceutical, biotechnology, or healthcare industry.
  • Exceptional written and verbal communication skills, including experience drafting executive-level content.
  • Proven experience developing presentations for senior executives using Microsoft PowerPoint and related business communication tools.
  • Strong analytical skills and the ability to synthesize technical or operational data into clear narratives.
  • Strong stakeholder management skills and the ability to build relationships with senior leaders and diverse teams.

Desired:

…

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