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Insmed

Develops therapies for rare diseases

Executive Director - Multiple Teams

Regulatory & Quality (Life Sciences)Updated on Nov 13
Full-timeRemote in USA

About the Job

Requirements

  • A bachelor's degree in a life sciences discipline is required.
  • At least 12 years of experience in pharmaceutical regulatory affairs, including at least 6 years focused specifically on labeling and advertising/promotional compliance.
  • Proven experience managing high-performing regulatory teams and working with senior executives.
  • Expert understanding of FDA regulations, guidance documents, and promotional enforcement actions, including Untitled and Warning Letters.
  • Exceptional writing, negotiation, and public-speaking skills.

Responsibilities

  • Provide strategic leadership to the Labeling, Advertising & Promotion Regulatory team by establishing accountabilities, priorities, operating models, performance expectations, and cross-functional interfaces.
  • Integrate labeling, advertising, and promotion activities to align approved product labeling, emerging clinical and safety information, promotional claims, and external product communications.
  • Ensure labeling, advertising, and promotional communications meet applicable global regulatory requirements and scientific standards while supporting corporate objectives.
  • Lead global labeling strategy, governance, lifecycle management, and implementation of product information changes across marketed and pipeline products.
  • Oversee review and approval of advertising and promotional materials to ensure compliance with applicable regulations, corporate standards, and policies while supporting business objectives.
  • Serve on the Global Regulatory Affairs leadership team as a strategic advisor to the SVP, Regulatory Affairs, and a senior partner to Commercial, Marketing, Medical Affairs, Legal, Compliance, Clinical Development, Drug Safety, Quality, and other relevant functions.
  • Lead health authority meetings and negotiations on labeling disputes and promotional compliance matters.
  • Ensure the team has the regulatory expertise, technical capabilities, staffing, and operational capacity to deliver its priorities.
  • Oversee resource planning, budget management, workload prioritization, and capability development; monitor performance, identify operational and compliance risks, and drive continuous improvement.
  • Lead, mentor, and empower regulatory professionals overseeing labeling and advertising and promotional materials, delegating effectively to maintain focus on strategic priorities and execution.
  • Develop leadership capabilities, establish succession plans, and foster a high-performing culture; define team roles, responsibilities, escalation pathways, and performance expectations.

Desired Qualifications

  • An advanced degree (PharmD, PhD, or MS) is preferred.
  • Global ex-U.S. labeling experience (EMA/EU) is a strong plus.

About the Company

Insmed

Develops therapies for rare diseases

Insmed focuses on developing and delivering therapies for serious and rare diseases. Its products come from a pipeline of clinical trials and approved treatments, sold to patients in global markets with offices in Bridgewater, NJ, Europe, and Japan. The company’s work combines research and development, regulatory approvals, and commercialization to bring therapies from discovery to patients. Insmed differentiates itself by addressing unmet medical needs in rare diseases and maintaining a global infrastructure that supports development, approval, and patient access. The goal is to improve patient outcomes by providing effective treatments for conditions with limited existing options.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Bridgewater Township, New Jersey
Founded
1988

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