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Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Global Regulatory Affairs, Strategy and Operations Co-op

Business OperationsConfirmed live in the last 24 hours
Internship · Winter 2027Boston, MA, USA$30 - $55 /hr

About the Job

Requirements

  • Currently enrolled in a business-focused graduate program, such as an MBA, MS in Management, Business Analytics, or Health/Biotech Management; or a science-focused graduate program, such as biology, chemistry, biochemistry, or pharmaceutical sciences, with business as a minor or second degree.
  • Enrolled in a formal co-op or experiential learning program and available full-time in an on-site or hybrid capacity in Boston for the full six-month assignment.
  • Advanced PowerPoint and Excel skills, including building executive-ready slides and data views.
  • Demonstrated ability to use technology to simplify or automate repeatable work, such as workflow tools or AI assistants.
  • Demonstrated ability to organize ambiguous work, collaborate with cross-functional stakeholders, and follow through without close supervision.
  • Strong written communication.
  • Sound judgment and discretion with confidential information.
  • Legal authorization to work in the United States, now and in the future; sponsorship is not provided for internships, co-ops, or entry-level roles within this part of the organization.
  • Must be enrolled in an advanced degree program if graduating before June 2027.
  • Must be available to work full-time, 40 hours per week, from January through June 2027.

Responsibilities

  • Help organize, develop, and drive key activities across Global Regulatory Affairs, including leadership team operating rhythms, department activities, recurring leadership reporting, and strategic initiatives.
  • Build automated, AI-enabled processes designed to run year-over-year with minimal manual involvement, a named owner, maintenance guidance, and testing through live cycles.
  • Own defined projects end to end and present projects and recommendations to the Global Regulatory Affairs leadership team at the end of the assignment.
  • Build an automated annual operating calendar of recurring leadership and departmental activities, linked to supporting materials and equipped with automated reminders and adjustable planning workflows.
  • Support recurring leadership team meetings by maintaining the forward agenda calendar, automating requests for topics and pre-reads, and using AI tools to draft pre-read summaries and meeting recaps for review.
  • Build a decision log and action tracker that automatically follows up with owners on open items and produces regular status reports.
  • Support planning and logistics for departmental activities, including offsite meetings, town halls, and department meetings.
  • Organize supporting materials into a structured repository with clear ownership and update conventions.
  • Support recurring leadership reports covering progress against annual goals, current organizational charts, and related activities.
  • Maintain current-state organizational charts, including reporting-line changes and integration-related moves, on a repeatable refresh cycle.
  • Contribute to monthly newsletters, including milestone updates, organizational announcements, and reminders.
  • Map recurring activities and reports against corporate activities, establish planning lead times and owners, and organize supporting materials into a maintained location.
  • Automate updates for recurring reports and activities, including scheduled, tracked workflows for offsite meetings, goal progress, organizational changes, hiring updates, and organizational health.
  • Support an active transition project with the Chief of Staff by developing work products and plans, tracking milestones, and creating content for integration activities as needed.
  • Deliver a working transition plan and reusable templates and trackers for future departmental transitions.

Desired Qualifications

  • Familiarity with Microsoft 365 Copilot or other AI productivity tools, and curiosity about applying them to real workflows.
  • Hands-on experience building workflows or dashboards in Power Automate, Power BI, or similar tools.
  • Exposure to the biotech, pharmaceutical, or broader healthcare sector, or interest in drug development or regulatory affairs.
  • Prior experience in consulting, corporate strategy, program management, business operations, or post-merger integration.
  • A regulatory affairs background is ideal but not required where there is strong interest in the discipline.

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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