Supply Chain Coordinator Boston

Celea Therapeutics, Inc.; Boston, Northern (MA, KY); Hybrid; USD 75,000 - 85,000; Full time

Job summary

Celea Therapeutics, Inc. in Boston is seeking an experienced Supply Chain Coordinator to execute study supply strategies from setup to closeout.

The role reports to the Associate Director Global Supply Chain and Logistics and centers on planning, forecasting, and coordinating supply activities for a Phase 3 study. The position focuses on packaging and distribution for a global Phase 3 study, with three days on site in Boston.

Qualifications

• Bachelor's degree in supply chain or related field preferred.
• 5+ years work experience with at least 3+ years in supply chain.
• Experience executing a supply strategy for a Global Phase 2 or 3 study.
• Track record of successful supply strategy execution.
• Entrepreneurial mindset and comfort operating in a fast-paced, early-stage environment.
• Proficiency using AI tools to work smarter—curiosity about technology improvements.

Responsibilities

• Clinical Supply Planning & Forecasting: develop study supply strategies and packaging plans.
• Inventory Management & IRT/RTSM Oversight: manage inventory in IRT/RTSM systems and reconcile data.
• Clinical Supply Operations: packaging, labeling, and distribution with CDMOs; ensure timely release.
• Logistics & Distribution: coordinate domestic and international shipments; manage import/export requirements.
• Process Improvement: develop and revise SOPs; implement AI/automation to scale processes.

Skills

Supply chain experience

Global study experience

AI tools familiarity

Fast-paced environment

Entrepreneurial mindset

Education

Bachelor's degree in supply chain or related field

Tools

IRT/RTSM systems

CDMO coordination tools

Job description

Celea Therapeutics is dedicated to advancing transformative treatments for people with serious respiratory diseases. Drawn from the Latin word for “sky,” our name reflects our mission to rise above the status quo and deliver therapies that change lives. Our lead program, deupirfenidone (LYT-100), is currently in Phase 3 clinical development with active candidate enrollment, representing a potential new standard of care for idiopathic pulmonary fibrosis (IPF) and other fibrotic lung diseases.

Rising above the status quo takes a team as strong as its science, and we hire and work by five values: accountability — owning outcomes and acting like owners; transparency — talking straight and building trust; collaboration — achieving together what no one could alone; innovation — challenging accepted ideas and taking smart risks; and passion — bringing energy and heart to the mission.

Position Overview

As we prepare for our next stage of growth and clinical advancement, Celea is seeking an experienced Supply Chain Coordinator to execute study supply strategies from initial study setup activities to eventual study closeout. They will be reporting to the Associate Director Global Supply Chain and Logistics.

In the near term, their focus will be the management of packaging and distribution activities for our global Phase 3 study, ensuring on time delivery per the study supply strategy. Over time, this person will aid the growth of the Celea study portfolio, providing supply chain support for new studies as they develop. They will be instrumental in guiding Celea through its next chapter.

This position is Boston based, with 3 days on site.

Key Responsibilities

Clinical Supply Planning & Forecasting

• Collaborate in the development of study supply strategies and packaging plan for assigned clinical programs
• Collate information from clinical supply systems reports to assist in monitoring study progress and inventory consumption/usage.

Inventory Management & IRT/RTSM Oversight

• Manage clinical inventory within IRT/RTSM systems and other supply management tools.
• Perform ongoing inventory reconciliation and ensure accurate product accountability.
• Monitor key supply metrics and proactively identify inventory risks or supply gaps.

Clinical Supply Operations

• Execute packaging and labeling activities with CDMO per study packaging plan.
• Ensure timely release and distribution of clinical supplies according to study strategy.
• Serve as the day-to-day operational contact for CDMOs, Clinical Operations, logistics providers, and other supply chain partners.
• Support monitoring of vendor performance against established timelines and service level expectations.
• Escalate performance issues and supply risks to the Associate Director as appropriate.

Logistics & Distribution

• Coordinate domestic and international clinical supply shipments.
• Support import/export activities, customs documentation, and country-specific distribution requirements.
• Monitor shipment status and resolve transportation issues in collaboration with logistics providers.
• Manage temperature-controlled shipping requirements and ensure product integrity throughout distribution
• Identify supply risks and develop mitigation plans to prevent interruptions to clinical studies.
• Ensure supply chain activities are conducted in compliance with GCP, GMP, GDP, and company procedures.
• Participate in deviation investigations, CAPAs, and change control activities as needed.

Process Improvement

• Support development, revision, and implementation of clinical supply chain SOPs and work instructions.
• Identify opportunities to improve supply chain efficiency, forecasting accuracy, inventory management, and operational execution.
• Build and continuously improve processes, standards, and tools — including thoughtful use of AI and automation — so the function scales with the company.

Qualifications

Required

• A bachelor's degree in supply chain, science, or a healthcare related field, or equivalent on-the-job work experience is preferred
• 5+ years work experience with at least 3+ years of experience in Supply Chain
• Demonstrated expertise in Supply chain activities, including the execution of a supply strategy for a Global Phase 2 or 3 study.
• Track record of successful supply strategy execution
• Entrepreneurial mindset and comfort operating in a fast-paced, early-stage environment.
• Proficiency using AI tools to work smarter — curiosity about how technology can improve the quality and speed of your work.

Preferred

• Experience in work within GxP Guidelines and adherence to SOPs
• Experience in the setup of distribution network for Phase II and III Global Trials
• Managing the supply chain aspects of IRT/IWRS builds and User Acceptance Testing
• Experience in development of Clinical Supply Planning Tools

Why Join Celea Therapeutics

• Play a pivotal role in advancing life-changing therapies for patients with devastating lung diseases.
• Shape the foundation of a Phase 3 biotech poised for significant growth.
• Collaborate with a passionate, mission-driven leadership team.
• Competitive compensation and equity package.

Compensation

Transparency is one of our values, and that includes how we pay. The anticipated salary range for this role is $75,000 – 8$5,000 plus bonus and equity. Where an offer lands within the range reflects the candidate’s experience, skills, and internal equity — and we welcome open conversations about compensation from the first call, so there are no surprises at the offer stage.

Actual compensation will be determined based on experience, qualifications, and location. In addition to base pay, this role is eligible for bonus and equity compensation.

Base Pay Information

$75,000 - $85,000 USD

Our Commitment

Celea Therapeutics is an equal opportunity employer. We evaluate every candidate against the requirements of the role using a structured, evidence-based process, and we make employment decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other legally protected characteristic.

For more information, visit www.celeatx.com or connect with us on Twitter @celeatx.