Associate Director, Clinical Supply Chain at Merida Biosciences

Cambridge, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

06 Aug, 26

Salary

240000.0

Posted On

08 May, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Supply Planning, Demand Forecasting, Vendor Management, IRT Strategy, Logistics Management, Temperature-Controlled Distribution, Packaging and Labeling, Clinical Trial Execution, Risk Mitigation, Budget Management, Regulatory Compliance, Supply Chain Operations

Industry

Biotechnology Research

Description

Description Associate Director, Clinical Supply Chain At Merida Biosciences, we are pioneering true precision medicines for antibody-driven diseases. We specifically target pathogenic antibodies and their cellular sources with bespoke Fc biotherapeutics engineered to selectively and eliminate the root causes of autoimmune and allergic diseases, and to achieve deep, durable responses while preserving essential immunity. We are looking for passionate individuals to join our mission to transform treatment paradigms across the spectrum of antibody-driven diseases. The Associate Director, Clinical Supply Chain will lead hands-on clinical supply planning and execution across global Phase 1 and Phase 2 studies. This role owns clinical supply operations through an outsourced network of packaging, depot, distribution, and logistics partners and works closely with Clinical Operations, CMC, Quality, and Regulatory to ensure uninterrupted and compliant study supply. The ideal candidate is a practical operator who can manage complexity, build fit-for-purpose processes, and execute effectively in a lean biotech environment. Key Responsibilities • Lead end-to-end clinical supply planning and execution for global clinical studies across investigational product and supporting clinical materials. · Develop and maintain demand forecasts and supply plans based on enrollment, dosing, regional activation, manufacturing lead times, and protocol changes. · Partner with Clinical Operations on IRT strategy and setup, including supply parameters, forecasting assumptions, and ongoing change control. · Define and manage depot strategy, distribution plans, and global shipping/logistics, including management of temperature-controlled distribution and external depot/logistics partners. · Manage external partners responsible for packaging, labeling, storage, and distribution of IMP and comparator/ancillary materials, including performance, timelines, budgets, and issue escalation. · Partner with Clinical Operations, CMC, Quality, and Regulatory to align supply plans with manufacturing, release, labeling, and study execution needs. · Author study pharmacy manuals in collaboration with Clinical Operations, CMC, and other functions as needed. · Support packaging and release readiness in partnership with Quality, including deviation/investigation support, temperature excursion assessment, and disposition planning as needed. · Identify supply risks early and drive practical mitigation plans to protect study continuity, compliance, and timelines. · Establish fit-for-purpose processes, reporting and governance for clinical supply activities appropriate for an emerging biotech organization. Requirements Required Qualifications · Bachelor’s degree in Life Sciences, Pharmacy, Engineering, or related field. · 8+ years supply chain experience in biotech or pharmaceutical organizations, including direct responsibility for global clinical trial supply execution. · Strong experience in demand forecasting, supply planning, and outsourced vendor management. · Experience supporting global or multi-region clinical studies. · Experience with packaging, labeling, depot oversight, and temperature-controlled distribution for clinical materials. · Demonstrated ability to operate independently and effectively in a lean biotech environment. Preferred Experience · Experience supporting clinical supply in complex import/export environments (e.g., China, Australia) and managing multi-country labels. · Experience with comparator and ancillary supply strategy and execution. · Experience supporting blinded studies and IRT-enabled supply planning. · Experience with frozen biologic or frozen drug product supply chains. · Experience in emerging biotech or start-up environments. Compensation: We understand that compensation is an important part of considering a new opportunity. Our goal is to be transparent so there are no surprises at the end of the process, and you can feel confident that your offer is both fair and equitable. To support that, we’re sharing our hiring range for this role upfront: typically for the Associate Director level we target $200,000 to $240,000 . The final offer will take into account a number of factors, including your skills, experience, location, market data, and internal equity. Along with a competitive salary, we’re proud to offer a comprehensive benefits package designed to support you both personally and professionally. Merida Biosciences is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited

Responsibilities

Lead end-to-end clinical supply planning and execution for global Phase 1 and 2 studies. Manage an outsourced network of packaging, depot, and logistics partners to ensure uninterrupted and compliant study supply.