---
title: 'Senior Manager, Clinical Supply Planning and Inventory Management at Amylyx Pharmaceuticals'
canonical: 'https://feeny.ai/job/senior-manager-clinical-supply-planning-and-inventory-management-amylyx-b97c7kp9pj39'
type: 'job'
last_seen: '2026-11-03'
---

# Senior Manager, Clinical Supply Planning and Inventory Management at Amylyx Pharmaceuticals

- **Company:** Amylyx Pharmaceuticals
- **Location:** Cambridge, MA
- **Compensation:** $144k–$162k
- **Posted:** 2026-10-27
- **Last confirmed live:** 2026-11-03
- **Apply:** https://job-boards.greenhouse.io/amylyx/jobs/6236309004

## Job description

Amylyx has an audacious mission to usher in a new era for treating diseases with high unmet needs. Where others see challenges, we see opportunities that we pursue with urgency, rigorous science, and unwavering commitment to the communities we serve. We are a clinical-stage company currently focused on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).

Our mission is powered by our people. Our core values – be audacious, be curious, be authentic, be engaged, and be accountable – creating a culture of caring. Amylyx has assembled an experienced team ready to take action because the communities we serve have no time to wait. If you share our passion and are determined to tackle some of medicine’s toughest problems, we encourage you to read the opportunity below and apply.

The Opportunity

The Senior Manager of Clinical Supply Chain Planning will be responsible for developing, managing, and executing end-to-end clinical supply strategies in support of global clinical studies across multiple phases of development. This role will oversee clinical supply forecasting, vendor coordination, systems transactions, compliance documentation, and risk mitigation to ensure uninterrupted supply of investigational product, placebos, and ancillary materials. The position requires close collaboration with Clinical Operations, CMC, External Manufacturing, Quality, Regulatory Affairs, Finance, depots, IRT providers, packaging and labeling vendors, logistics partners, and other cross-functional stakeholders.

## Responsibilities

Clinical Supply Planning and Execution

- Build and manage clinical supply strategies and supply plans for assigned products, including RSMs, API, bulk drug product, finished goods, investigational product, comparators, placebos, and ancillary materials.
- Create, maintain, and communicate clinical supply forecasts based on study enrollment assumptions, protocol design, adoption projections, manufacturing schedules, packaging and labeling plans, distribution needs, and inventory requirements.
- Lead supply planning activities, including demand forecasting, inventory management, packaging, labeling, distribution, resupply strategies, and scenario planning.
- Conduct demand and supply analyses to ensure forecasted requirements can be fulfilled within study timelines and operational constraints.
- Monitor clinical supply levels and proactively identify and mitigate material supply constraints or risks that may impact study timelines.
- Support clinical study closeout(s) by managing supply accountability, inventory reconciliation, and inspection readiness preparations.

Cross-Functional and Vendor Collaboration

- Serve as the clinical supply chain representative on clinical study teams, internal and external operations meetings, and cross-functional project teams.
- Partner with Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, CMC, External Manufacturing, Quality, Finance, and external partners to align supply plans with clinical development objectives.
- Partner with Analytical Development to manage expiry extensions and dispositioning of expired inventory at CMO locations.
- Participate in protocol review activities and assess the supply chain impact of study design changes.
- Manage relationships with CMOs, CTM vendors, depots, packaging and labeling vendors, IRT providers, logistics partners, and other external service providers.
- Create, track, and manage purchase orders and change orders for supply chain planning-related activities.

Quality, Compliance, and Continuous Improvement

- Ensure clinical supply activities comply with applicable GxP regulations, company policies, clinical trial regulations, and industry best practices.
- Own or support applicable change controls, deviations, CAPAs, SOPs, and other quality documentation within the QMS.
- Author and maintain supply chain SOPs and support technical writing for clinical pharmacy manuals and related controlled documents.
- Support internal and external audits, inspections, and inspection readiness preparations.
- Identify supply chain risks, lead contingency planning, and implement process improvements to enhance efficiency, scalability, compliance, and operational performance.

Inventory Management

- Track inventory at all CMO (contract manufacturing organization) locations and reconcile inventory discrepancies. Collect month-end inventory balance reports for all Amylyx partner locations to reconcile with Amylyx Accounting team at each month-end.
- Manage both manual and system-driven inventory reporting.
- Provide ad-hoc inventory analysis. Experience with genealogy tracking/recall best practices is a plus.
- Support CMO inventory KPI’s to drive continuous improvement.
- Own master data in clinical supply chain operating systems to maintain accurate safety stock inventory, item lead time, sourcing rules, lot tracking, etc.
- Transact inventory movements in applicable supply chain operating systems (ex. IRT)
- Collaborate cross functionally to establish user clinical system requirement specs, complete UAT, and perform system transactions.

Required Qualifications

- 5+ years of relevant experience in the Pharmaceutical Industry; or a BS degree and minimum 4+ years of relevant experience; or a MS degree and minimum 3 years of relevant experience.
- Demonstrated experience in clinical supply planning, forecasting, inventory management, packaging, labeling, distribution, and logistics.
- Experience managing external vendors, CMOs, depots, IRT providers, logistics partners, and other contract organizations.
- Strong understanding of GxP requirements, GMP/GCP expectations, clinical trial regulations, and quality systems.
- Proficiency with clinical supply management systems, IRT systems, ERP platforms, QMS systems, Microsoft Office applications, Excel, and Smartsheet.
- Strong project management, organizational, analytical, communication, presentational, collaboration, and stakeholder management skills.
- Ability to work effectively in a fast-paced, multi-disciplinary team environment.

## Preferred Requirements

- Experience in a small to mid-sized biotech environment.
- Experience supporting rare disease, neuroscience, or specialty pharmaceutical programs.
- Experience with Suvoda, NetSuite, Veeva, or similar clinical supply, ERP, or QMS platforms.
- Technical writing experience related to SOPs, clinical pharmacy manuals, or other controlled documents.
- Experience with global supply networks, international distribution, genealogy tracking, and recall-readiness best practices.

Work Location and Conditions

- At Amylyx, we proudly support remote work opportunities within the United States. However, due to business considerations related to health insurance coverage and state tax regulations, we are unable to hire employees who reside and/or work in certain states. Currently, we are not considering applicants from Alaska and Hawaii.
- You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested.
- You must have access to work in setting which enables meeting all requirements of the role (including privacy, reliable internet access, phone, ability to video conference, etc.) at your remote location.

## Compensation

The pay range posted below represents our good faith estimate of compensation for this role, based on market data and internal benchmarks. The final offer may vary depending on a candidate’s experience, skills, and qualifications, as well as considerations of internal equity.

Estimated Pay Range $144,000—$162,000 USD

To stay connected with us, follow Amylyx Pharmaceuticals on [LinkedIn](https://www.linkedin.com/company/amylyx).

To return to our website please [click here](https://www.amylyx.com/).

Amylyx Pharmaceuticals is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, pregnancy-related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances. Amylyx’s management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities, access to facilities and programs, and general treatment during employment. Accommodations are available for candidates who require them in our selection process. If you need an accommodation, please let your Amylyx Talent Acquisition contact know.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

## About Amylyx Pharmaceuticals

## Company Overview
- **One-liner**: Amylyx Pharmaceuticals is a clinical-stage pharmaceutical company focused on developing novel therapies for serious diseases with high unmet needs, including neurodegenerative and rare diseases.
- **Entity Type**: Public (NASDAQ: AMLX)
- **Headquarters**: Cambridge, Massachusetts, United States
- **Founded**: 2013
- **Founders**: Josh Cohen and Justin Klee

## Core Business
- Primary industry/industries: Biotechnology / Pharmaceuticals
- Target customers: Patients, healthcare providers, and payers (B2B/B2C); primarily focused on rare and neurodegenerative diseases
- Mission or purpose statement: To develop novel therapies for high unmet needs with urgency, rigorous science, and unwavering commitment to the communities they serve.

## Products & Services
- **AMX0035 (RELYVRIO®/ALBRIOZA)**: An investigational combination therapy for Wolfram syndrome and previously approved for ALS (voluntarily withdrawn after Phase 3 PHOENIX trial did not meet primary endpoint). Still being studied in Wolfram syndrome.
- **Avexitide**: A Phase 3-ready GLP-1 receptor antagonist with FDA Breakthrough Therapy designation for post-bariatric hypoglycemia (PBH) and congenital hyperinsulinism (HI). Dosing in Phase 3 LUCIDITY trial.
- **AMX0114**: An investigational therapy for ALS, currently in Phase 1 LUMINA clinical trial, with FDA Fast Track designation.
- **AMX0318**: A long-acting GLP-1 receptor antagonist in IND-enabling studies for PBH and other rare diseases, developed in collaboration with Gubra A/S.

## Market Standing
- **Valuation/Market Cap**: Not publicly available from provided sources (public company; market cap fluctuates)
- **Key Metric**: Completed IPO on NASDAQ in April 2025 (ticker: AMLX); annual revenue not disclosed (clinical-stage, no approved products currently marketed)
- **Notable Investors/Partners**: Gubra A/S (research collaboration), Dr. Rudy Tanzi (Founding Chair of Scientific Advisory Board)
- **Growth Signals**: Expanded pipeline with avexitide acquisition (July 2024); multiple FDA designations (Fast Track, Orphan Drug); first patients dosed in Phase 1 LUMINA (ALS) and Phase 3 LUCIDITY (PBH); ongoing IND-enabling studies for AMX0318.

## Competitive Advantages
- Focus on high unmet needs with a rigorous, science-driven approach to drug development.
- Strong pipeline diversification across multiple rare and neurodegenerative diseases.
- Experienced team with collective expertise from therapeutic development through commercialization.
- Deep engagement with patient communities and care providers to understand unmet needs.
- Agile, hybrid-remote work environment that attracts and retains top talent.

## Strategic Focus
- Advancing late-stage clinical trials (avexitide Phase 3, AMX0035 Phase 2 in Wolfram syndrome).
- Expanding pipeline through business development and collaborations (e.g., Gubra).
- Leveraging regulatory designations (Breakthrough Therapy, Fast Track, Orphan Drug) to accelerate development.
- Continuing to build a culture of urgency, accountability, and innovation to serve patients with high unmet needs.

## Why Work Here
- **Culture**: Values-driven environment emphasizing accountability, audacity, authenticity, curiosity, and engagement. Rooted in connection with colleagues and the communities served.
- **Work Model**: Hybrid-remote with headquarters in Cambridge, MA. Three annual Anchor Weeks in-person and bi-weekly Amylyx Exchange meetings for connection.
- **Benefits**: Flexible PTO, 5% 401(k) employer contribution, paid parental leave, medical/dental/vision, HSA/FSA, employee assistance program, mobile reimbursement, learning and development program, recognition platform.
- **Engineering/Research Culture**: Emphasis on rigorous science, continuous learning, and generous knowledge sharing. Opportunities to work on cutting-edge therapies from preclinical through commercialization.

## Sources
1. [Amylyx Pharmaceuticals - Our Company](https://www.amylyx.com/our-company)
2. [Amylyx Pharmaceuticals - Careers](https://www.amylyx.com/careers)
3. [Amylyx Pharmaceuticals - Homepage](https://www.amylyx.com/)
4. [Jobs at Amylyx Pharmaceuticals - Greenhouse](https://job-boards.greenhouse.io/amylyx)
5. [Open Positions - Amylyx Pharmaceuticals](https://www.amylyx.com/open-positions)

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