Strategic Publications Lead, Market Access & Evidence

Takeda Pharmaceutical Company Limited

Boston (MA)

On-site

USD 169,000 - 266,000

Full time

7 days ago
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Job summary

Takeda Pharmaceutical Company Limited in Boston seeks an Associate Director to shape publication strategies and translate evidence into high-quality communications that support market access. You will collaborate across Medical Affairs, Evidence Generation, and Global/Regional Market Access to produce publications and AI-enabled content that meets regulatory standards.

You will lead planning for abstracts, manuscripts, congress presentations, and plain-language summaries, while mentoring teams

Qualifications

  • Bachelor's degree in life science or healthcare
  • 6+ years in biopharma or related field
  • 3+ years in scientific publications/publication planning
  • Knowledge of drug development, trial design, biostatistics, and reporting

Responsibilities

  • Develop and execute publication strategies
  • Lead publication planning for abstracts, manuscripts, congress presentations, and summaries
  • Partner with cross-functional teams to align priorities and timelines
  • Ensure publication quality and compliance with standards
  • Create reusable evidence resources and derivative content
  • Apply AI-enabled technologies to improve planning and content development
  • Monitor publication performance and incorporate insights
  • Oversee budgets, timelines, vendors, risks, and mentoring

Skills

Publication strategy
Cross-functional leadership
AI-powered publications
Scientific communication
Stakeholder influence
Mentoring

Education

Bachelor's degree in life science or healthcare

Job description

Takeda Pharmaceutical Company Limited in Boston seeks an Associate Director to shape publication strategies and translate evidence into high-quality communications that support market access. You will collaborate across Medical Affairs, Evidence Generation, and Global/Regional Market Access to produce publications and AI-enabled content that meets regulatory standards.

You will lead planning for abstracts, manuscripts, congress presentations, and plain-language summaries, while mentoring teams

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