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Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Associate Director - HCP Marketing & Speaker Bureau, US Kidney

Brand & Creative MarketingConfirmed live in the last 24 hours
Full-timeBoston, MA, USA

About the Job

Requirements

  • A bachelor's degree is required.
  • Typically, 7+ years of experience in healthcare, biopharmaceuticals, pharmaceutical marketing, speaker bureau, thought leader engagement, content development, or agency roles is required.
  • Experience developing promotional, disease education, or peer-to-peer content in regulated environments is required.
  • Experience managing agency partners, content review processes, and cross-functional workstreams is required.
  • Strong content development and project management skills are required.
  • Ability to translate strategic direction into executable content workstreams is required.
  • Strong agency management, including timeline and deliverable tracking, is required.
  • Attention to detail around references, content accuracy, and approval requirements is required.
  • Ability to manage multiple projects, timelines, and stakeholders simultaneously is required.
  • Cross-functional collaboration with Marketing, Medical, Sales, Regulatory, Legal, Compliance, Operations, and agency partners is required.
  • Comfort in fast-paced launch environments is required.
  • Understanding of compliant content development in regulated biopharmaceutical settings is required.
  • Ability to travel approximately 30%, including weekends, for speaker trainings, internal meetings, agency meetings, and select field or program activities is required.

Responsibilities

  • Lead day-to-day development of peer-to-peer educational content across the US Kidney franchise, initially emphasizing AMKD.
  • Support development of speaker decks, training materials, discussion guides, frequently asked questions, and field resources.
  • Partner with agency teams to manage content timelines, drafts, revisions, and version control.
  • Ensure content aligns with the strategic narrative, educational objectives, and franchise priorities.
  • Support preparation of materials for internal review, including references and supporting documentation.
  • Serve as executional lead for AMKD content development and establish content infrastructure for peer-to-peer education.
  • Translate AMKD strategic priorities into clear content workstreams, timelines, and deliverables.
  • Coordinate with stakeholders and agency partners to develop AMKD disease education and branded materials.
  • Identify content gaps, update needs, and opportunities to strengthen the educational platform.
  • Support movement of materials through Medical, Regulatory, Legal, Compliance, and other required reviews.
  • Capture reviewer feedback, manage follow-ups, coordinate agency revisions, and ensure appropriate resolution.
  • Maintain content trackers, review timelines, reference documentation, and approval status.
  • Ensure materials comply with company policies and review requirements.
  • Support the speaker bureau through content readiness, speaker materials, and training resource development.
  • Develop speaker training materials, run-of-show documents, and speaker communications.
  • Work closely with Marketing, Medical, Sales, Regulatory, Legal, Compliance, Operations, and agency partners.
  • Manage agency deliverables, timelines, and executional follow-through.
  • Maintain visibility through status updates, project trackers, and milestone planning.

Desired Qualifications

  • An advanced degree is preferred.
  • Rare disease, nephrology, immunology, specialty medicine, or launch experience is preferred.
  • Speaker bureau or key opinion leader engagement experience is preferred.
  • Kidney experience or speaker bureau experience, plus a scientific terminal degree such as a PharmD or PhD, is strongly preferred.

About the Company

Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Vertex Pharmaceuticals develops medicines for serious diseases, with a focus on cystic fibrosis. It conducts extensive research and partners with other biotech firms to discover and develop new therapies, including ex vivo engineered cell treatments. Its products, such as ivacaftor, treat cystic fibrosis and other therapies undergo clinical testing to expand the pipeline. Revenue comes from selling approved drugs and from licensing and collaboration agreements. The company distinguishes itself through deep R&D investment, strategic partnerships, and a global reach aimed at addressing unmet medical needs. The overall goal is to bring effective new drugs to patients worldwide and improve outcomes and quality of life.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Boston, MA
Founded
1989

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