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Insmed

Develops therapies for rare diseases

Compliance Manager - Clinical Supply Chain

Regulatory & Quality (Life Sciences)Updated on Nov 13
Full-timeBridgewater, NJ, USA

About the Job

Requirements

  • A bachelor's degree and at least five years of experience in drug development, clinical supply chain management, and/or clinical manufacturing operations.
  • Ability to identify process-management risks and develop operationally achievable solutions.
  • Proficiency with Microsoft Excel, PowerPoint, and Word.
  • Experience working with and/or managing external vendors.
  • Working knowledge of Good Manufacturing Practice, Good Clinical Practice, and International Council for Harmonisation guidelines.
  • Ability to handle multiple projects simultaneously.

Responsibilities

  • Ensure audit readiness for potential inspections supporting Clinical Supply Chain and Technical Operations, and serve as the main compliance contact for designated clinical supply studies and projects.
  • Assist in developing the Trial Master File index to support the supply chain for assigned studies and programs.
  • Support Interactive Response Technology system design and user acceptance testing requirements for assigned studies, and perform user acceptance testing on those systems.
  • Support change control management activities within the clinical supply chain.
  • Coordinate with and manage external packaging, labeling, and distribution vendors.
  • Represent Supply Chain and Logistics in cross-functional study-level meetings, ensuring timely updates and information for assigned studies and projects.
  • Communicate relevant project information to internal and external stakeholders.
  • Develop and present slide decks, coordinate report drafting, and edit documents in preparation for business development activities.
  • Identify, report, manage, and mitigate clinical supply chain risks.
  • Provide regular updates to the Trial Master File in accordance with regulatory requirements.
  • Work with internal stakeholders to ensure supply compliance at each node in the supply chain.
  • Coordinate with Supplier Relationship Management for clinical suppliers, including maintaining key performance metrics.
  • Coordinate with contracted clinical supply organizations to appropriately disposition clinical supply material.
  • Draft standard operating procedures, work practices, and procedures for clinical trial material packaging, labeling, and distribution to ensure compliance with current Good x Practice requirements.
  • Work with supply chain colleagues to ensure consistency across processes and tools and implement improvements that produce sustainable results.
  • Manage the group's training curriculum.

Desired Qualifications

  • Experience with Microsoft Project and other computer software for demand- and supply-related systems.

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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