Consultant, Clinical Supplies Management, Biopharma, Global Trials
Anywhere
Type: Contract
Category: Manufacturing & Supply Chain
Industry: Life Sciences
Workplace Type: Remote
Reference ID: JN -082026-108303
Date Posted: 08/17/2026
Shortcut: http://careers.eliassen.com/xSiHg7
Description
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Description:
CONTEXT & INITIATIVE DESCRIPTION
Our BioPharma Client is seeking a Consultant, Clinical Supplies Management to support the planning and execution of global Phase I-III clinical trials. This critical Consultant will play a key role in ensuring the timely availability, packaging, distribution, and ongoing management of clinical trial supplies across sites and depots.
The ideal candidate will have strong clinical supply and trial operations experience, excellent cross-functional communication skills, and the ability to coordinate effectively across internal teams, vendors, logistics providers, and clinical sites.
This role will report into our client's Head of Clinical Supplies.
Responsibilities:
DUTIES/EXPECTATIONS:
Lead day-to-day operations related to clinical trial inventory, packaging, logistics, and distribution
Support forecasting and development of monthly supply and demand requirements to ensure clinical sites have the materials necessary to meet study needs
Develop and support supply planning and distribution strategies based on study requirements and enrollment forecasts
Assist with the management and distribution of ancillary clinical trial supplies as needed
Manage the translation of required clinical trial materials and coordinate review and approval with appropriate functions
Work cross-functionally with Clinical, Finance, Quality, Regulatory, and other relevant stakeholders to ensure effective communication and execution
Manage and/or oversee Interactive Response Technology (IRT) activities related to clinical supply management
Support vendor management and coordination to ensure timely completion of key milestones and deliverables
Partner with logistics providers to coordinate the timely delivery of clinical trial materials to sites and depots
Support the assessment, management, and release of temperature-related excursions affecting clinical sites and depots
Identify potential supply and distribution risks and work proactively with cross-functional teams and vendors to resolve issues
Provide ongoing operational support to ensure clinical supply activities remain aligned with study timelines and clinical needs
Experience Requirements:
MUST HAVES - QUALIFICATION SUMMARY
Minimum 3 years, Ideally 6+ years of relevant experience in clinical trial supply, clinical operations, or related
Experience supporting or managing global Phase 1-3 clinical trials
Experience managing or overseeing IRT systems and processes
Demonstrated experience with clinical trial supply forecasting, inventory management, logistics, and distribution
Experience working cross-functionally internal (Clinical, Quality, Regulatory) and with external vendors
Strong vendor and stakeholder management skills
Excellent organizational, communication, and problem-solving abilities
Ability to manage multiple priorities and operate effectively in a fast-paced clinical development environment
NICE-TO-HAVES
Experience supporting or managing clinical trials in China
Experience working with medical devices or device-related clinical trials
TRAVEL & LOCATION
REMOTE.
START & TERM
Immediate Start. 6 month initial contract with high likelihood to extend
Recruitment Transparency Notice
Eliassen Group values transparency in our recruitment practices. Please be advised that Eliassen Group utilizes artificial intelligence (AI) tools as part of its initial application screening and hiring process. You may receive email and SMS notifications from the Eliassen Virtual Recruiting Team ( [email protected] , 781-808-2924) inviting you to complete a brief voice screening as part of your application process. These tools assist our hiring teams in different ways, including but not limited to, assistance in reviewing application materials to help identify candidates whose qualifications most closely match the requirements of the position. All AI-assisted evaluations and responses are reviewed by human recruiters before any hiring decisions are made. The use of AI in our process is intended to support fairness, efficiency, and consistency, and Eliassen Group takes measures to prevent bias or discrimination in connection with its hiring practices. By proceeding, you acknowledge, agree, and consent to Eliassen Group's use of these tools, including AI tools, as part of the application and hiring process.
Skills, experience, and other compensable factors will be considered when determining pay rate. The pay range provided in this posting reflects a W2 hourly rate; other employment options may be available that may result in pay outside of the provided range.
W2 employees of Eliassen Group who are regularly scheduled to work 30 or more hours per week are eligible for the following benefits: medical (choice of 3 plans), dental, vision, pre-tax accounts, other voluntary benefits including life and disability insurance, 401(k) with match, and sick time if required by law in the worked-in state/locality.
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About Eliassen Group:
Eliassen Group is a strategic consulting firm that helps organizations reach further and achieve more through our technology, business advisory, and life sciences solutions. For nearly 40 years, we have combined exceptional people, deep domain expertise, and intelligent capabilities to expand our clients' capacity and accelerate meaningful outcomes. We are driven by a purpose to positively impact the lives of our employees, clients, consultants, and the communities we serve.
Eliassen is committed to building a diverse and inclusive team from a variety of backgrounds, perspectives, and skills. We are an Equal Opportunity and Affirmative Action Employer and all employment decisions are based on merit, performance, and business needs. Eliassen does not discriminate on the basis of race, color, gender identity or expression, sexual preference or orientation, sex (including pregnancy, childbirth, and related medical conditions), marital status, creed, religion, physical or mental disability, genetic information, military or veteran status, age, ancestry, national origin, citizenship status, prohibited criminal record inquiries of applicants and employees, or any other category protected by federal, state, or local laws.
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