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Amylyx Pharmaceuticals

Biopharmaceutical company developing neurodegenerative therapies

Vice President, Clinical Compliance and Systems

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in USA

About the Job

Requirements

  • A bachelor's degree in a scientific, healthcare, technology, business, or related discipline is required; an advanced degree is preferred.
  • Typically 15 or more years of progressive experience within Clinical Operations, Clinical Quality/Compliance, Clinical Systems, or related functions in the biotechnology or pharmaceutical industry.
  • Significant leadership experience building, leading, and developing teams and organizational capabilities.
  • Deep knowledge of clinical development and clinical trial execution, including applicable global regulations, ICH-GCP requirements, and ICH E6(R3).
  • Ability to translate business and operational needs into scalable processes, systems, and technology solutions.
  • Strategic thinking and judgment to balance regulatory requirements, operational needs, innovation, risk, and organizational priorities.
  • Communication and influencing skills to collaborate with senior leaders and stakeholders across scientific, operational, technical, and corporate functions.
  • Ability to operate effectively in a dynamic, fast-paced, entrepreneurial biotechnology environment and move between strategy and hands-on execution.
  • Commitment to developing people, building strong teams, and creating an inclusive and collaborative working environment.
  • Ability to work remotely in a setting that enables role requirements, including privacy, reliable internet access, phone, and video conferencing.

Responsibilities

  • Provide strategic leadership and vision for the Clinical Compliance and Clinical Systems functions within Clinical Operations, establishing scalable capabilities to support the clinical portfolio.
  • Build, lead, develop, and mentor a high-performing team responsible for clinical compliance, Trial Master File oversight, clinical systems, and related capabilities.
  • Establish the long-term strategy and roadmap for Clinical Compliance and Clinical Systems, sequencing investments in alignment with Clinical Operations and broader Development priorities.
  • Lead clinical compliance activities supporting company-sponsored clinical trials in accordance with applicable regulations, ICH-GCP requirements, internal standards, and industry best practices.
  • Establish and maintain an inspection-readiness framework, partnering across functions to ensure ongoing preparedness for regulatory inspections and audits.
  • Provide strategic oversight and governance of the electronic Trial Master File environment, including processes, standards, quality, completeness, and inspection readiness.
  • Partner with Clinical Operations and cross-functional stakeholders to modernize clinical processes, standard operating procedures, work instructions, templates, and supporting tools, including implementation of requirements associated with evolving regulatory standards such as ICH E6(R3).
  • Develop and execute a business capability roadmap for clinical and data-enabled operations, identifying technology-enabled capabilities for efficient, scalable, and compliant clinical trial execution.
  • Lead the evolution of clinical technology infrastructure, including the electronic Trial Master File, Clinical Trial Management System, reporting and dashboard capabilities, and other clinical platforms and tools.
  • Establish governance, ownership, standards, and processes across Clinical Systems with cross-functional stakeholders to promote data quality, consistency, usability, and cross-study visibility.
  • Partner with IT and other stakeholders on system selection, implementation, integration, validation, security, change management, and ongoing lifecycle management.
  • Evaluate emerging technologies and opportunities for digital innovation, automation, analytics, and responsible use of artificial intelligence within Clinical Operations.
  • Partner with Clinical Business Operations, Global Site Services, Clinical Program and Study teams, and other Clinical Operations leaders to support evolving internal, hybrid, functional service provider, and outsourced operating models.
  • Establish metrics, dashboards, and other mechanisms to assess compliance, system performance, operational effectiveness, risks, and opportunities for continuous improvement.
  • Anticipate future organizational and infrastructure needs as the clinical portfolio grows and translate them into scalable solutions.
  • Serve as a senior Clinical Operations leader and trusted advisor, contributing to the evolution of the function and fostering cross-functional relationships.
  • Promote a culture of quality, collaboration, innovation, continuous improvement, and patient focus.
  • Travel to the corporate location in Cambridge, Massachusetts several times a year and attend other company-related events as necessary and requested.

Desired Qualifications

  • An advanced degree.

About the Company

Amylyx Pharmaceuticals

Biopharmaceutical company developing neurodegenerative therapies

Amylyx Pharmaceuticals develops treatments for neurodegenerative diseases, with a focus on ALS and Alzheimer's disease. Its main asset is AMX0035, currently in clinical trials, including the CENTAUR study for ALS and the PEGASUS study for late mild cognitive impairment or early dementia due to Alzheimer’s disease. The company advances products through rigorous, randomized, double-blind, placebo-controlled trials to demonstrate safety and efficacy before pursuing commercialization. In addition to research, Amylyx engages in awareness and community campaigns to support patients, caregivers, and researchers. The company aims to bring validated therapies to market to improve patient outcomes and generate revenue by selling treatments to healthcare providers and patients.

Company size
51-200
Company stage
IPO
Headquarters
Cambridge, MA
Founded
2013

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