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Clinical Supply Manager Jobs (NOW HIRING)

Almac Group

Clinical Supply Manager

Souderton, PA · Hybrid

The Clinical Supply Manager is responsible for the successful execution of clinical supply projects; this includes communicating and driving timelines both internally and externally, working with, or ...

Kelly Services

Clinical Supply Manager

Rochester, NY

$47/hr

Kelly Science & Clinical has a new, temporary opportunity for a Clinical Supply Manager in Rochester, NY! Shift: Monday - Friday 8am-5pm A 4 month temporary opportunity with possibility to extend ...

CPC

Drug Supply/Clinical Trial Supply Manager

Aurora, CO · Remote

$70K - $90K/yr

Clinical Supply Management (General) * Establish and document supply chain for each project according to required scope * Manage supply planning/forecasting to ensure alignment with study activity ...

Vaxcyte

Senior Manager, Clinical Supply

San Carlos, CA · Hybrid

$158K - $185K/yr

Summary: Vaxcyte is seeking a Sr. Manager, Clinical Supply, to lead clinical demand and supply planning, along with the planning and execution of clinical packaging runs. This role will be ...

Verastem

Associate Director Clinical Supply

Needham, MA · On-site

$175K - $200K/yr

This role supports all aspects of clinical supply management, including investigational medicinal product (IMP) and comparator sourcing, demand forecasting, packaging and labeling, distribution ...

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How much do clinical supply manager jobs pay per year?

As of Aug 14, 2026, the average yearly pay for clinical supply manager in the United States is $106,193.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $135,000.00 per year, depending on experience, location, and employer.

What are the typical daily responsibilities of a clinical supply manager in a clinical trials environment?

As a Clinical Supply Manager, your daily tasks involve forecasting supply needs, coordinating with vendors and internal stakeholders, managing inventory levels, and ensuring timely delivery of clinical materials to trial sites. You'll work closely with clinical operations, quality assurance, and logistics teams to maintain regulatory compliance and address supply challenges. Regular monitoring of shipment status, documentation, and problem-solving are key aspects of the role. This position requires balancing multiple priorities to support the seamless execution of ongoing and upcoming clinical trials.

What is a clinical supply manager?

A Clinical Supply Manager oversees the planning, sourcing, distribution, and management of clinical trial materials to ensure they are available on time and in the correct quantities. They work closely with clinical operations, manufacturing, and logistics teams to maintain supply chain efficiency while adhering to regulatory requirements. Their responsibilities include demand forecasting, inventory management, and troubleshooting supply issues to prevent trial delays. Effective coordination and problem-solving skills are essential in this role to support successful clinical research outcomes.

What are the key skills and qualifications needed to thrive as a clinical supply manager?

To thrive as a Clinical Supply Manager, you need expertise in supply chain management, knowledge of clinical trial processes, inventory control, and often a bachelor's degree in life sciences, pharmacy, or a related field. Proficiency with clinical trial management systems (CTMS), supply forecasting tools, and familiarity with regulatory compliance such as GxP standards are typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for successful collaboration with clinical teams and vendors. These capabilities are vital to ensure uninterrupted clinical trial supply, regulatory adherence, and efficient project execution.

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Clinical Supply Manager jobs near you
Infographic showing various Clinical Supply Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $106,193 per year, or $51.1 per hour.

Clinical Supply Manager

Vera Therapeutics, Inc.

Brisbane, CA • On-site

Full-time

Re-posted 29 days ago

Job description

Position Summary:

The Clinical Supply Manager will report to the Senior Director of Clinical Supply Chain and will be responsible for carrying out operational activities of the clinical supply chain including logistics, manufacturing, distribution and inventory management of clinical supplies. Working with third-party packaging suppliers, Regulatory Affairs, Quality Assurance, CMC, and the Clinical Operations team, this position will be responsible for ensuring uninterrupted supply in the clinical trials.

Responsibilities:

  • Work with Clinical Operations to define the supply strategy for clinical study investigational medicinal product (IMP) in line with the study protocol.
  • Represent the Clinical Supply Chain on Clinical Study Teams (CST) and provide a high-level service to internal stakeholders (e.g. Clinical Operations, Regulatory, Quality, CMC).
  • Forecast IMP demand for global studies based on clinical study protocol and clinical study plan.
  • Collaborate with other members of CMC to ensure on-time delivery of IMP and adequate inventory levels of clinical supplies for the entire duration of the trials.
  • Create, monitor, and adapt supply plans to supply clinical study demand.
  • Initiate and oversee the generation, proofing, and translation of clinical study labels, as required.
  • Oversee IMP shipments within the global distribution network and prepare documentation for import and export of clinical supplies to depots and study sites, as required.
  • Coordinate drug returns from site back to depot and perform study drug reconciliation at study closeout.
  • Manage vendors for all labeling/packaging, distribution operations, and supporting services for Vera programs.
  • Manage comparator sourcing activities to ensure uninterrupted supply for clinical study.
  • Support IRT design for drug modules, perform user acceptance testing, develop IRT supply strategy (DNX parameters), and oversee ongoing supply activities in system.
  • Maintain audit readiness through eTMF filing and documentation practices.
  • Lead cross functional projects and process improvements related to drug supply.
  • Creates and/or revise process documents such as Standard Operating Procedures.
  • Additional responsibilities as required.

Qualifications:

  • Bachelor's or Master's degree in Business Administration, Operations Management, or a related field required.
  • Minimum of 5 years of progressive experience in supply chain, preferably within the biotech, pharmaceutical, or CRO industry.
  • Working knowledge of Good Manufacturing Practices (GMP), Good Clinical Practice (GCP), and Good Distribution Practice (GDP) is required
  • Ph3 Global study start up experience required
  • Comparator Sourcing experience required
  • Experience with IRT systems required

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