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Clinical Supply Jobs (NOW HIRING)

Crescent Biopharma

$210 - $240/hr

We are seeking a Director, Clinical Supply Chain to own clinical supply chain as we advance pa multi-program portfolio from Phase 1 to Phase 3. You will ensure clinical supplies gets from ...

Vaxcyte

Senior Manager, Clinical Supply

San Carlos, CA · On-site

$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 ...

Alkermes

Associate Director, Clinical Supply Chain

Waltham, MA · On-site

$196K - $222K/yr

The Associate Director position within Clinical Supply Chain provides strategic leadership and oversight for end-to-end supply chain management across multiple clinical programs as part of a growing ...

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Clinical Supply information

See salary details

$14

$34

$90

How much do clinical supply jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical supply in the United States is $34.62, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $32.93 per hour, depending on experience, location, and employer.

What is a clinical supply?

Clinical supply jobs involve managing the planning, sourcing, packaging, labeling, distribution, and inventory of medical products and supplies necessary for clinical trials. Professionals in this field ensure that study drugs and materials are delivered to clinical sites in the right quantity, at the right time, and under compliant conditions. These roles are essential for supporting clinical research and maintaining regulatory adherence throughout the supply chain.

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

To thrive as a Clinical Supply professional, you need expertise in supply chain management, knowledge of clinical trial processes, and often a background in life sciences or logistics. Familiarity with inventory management systems, clinical trial management software (CTMS), and regulatory compliance tools is crucial. Strong organizational skills, attention to detail, and effective communication are essential soft skills for success in coordinating supplies and collaborating with internal and external stakeholders. These competencies ensure the timely and compliant delivery of clinical materials, which is critical to the success of clinical trials.

What are some common challenges faced by professionals in clinical supply roles, and how are they typically addressed?

Professionals in Clinical Supply often face challenges such as managing tight timelines, coordinating logistics for global trials, and ensuring regulatory compliance across multiple countries. Balancing the demand for investigational products with unpredictable patient enrollment can also be complex. These challenges are typically addressed through meticulous planning, strong collaboration with clinical operations and regulatory teams, and leveraging specialized supply chain management software to track inventory and shipments. Effective communication and adaptability are key skills for overcoming these obstacles.

What is the difference between Clinical Supply vs Clinical Trial Coordinator?

AspectClinical SupplyClinical Trial Coordinator
Required CredentialsTypically a bachelor's degree in life sciences, pharmacy, or related field; experience in supply chain or logisticsBachelor's degree in health sciences, nursing, or related field; often requires clinical research certifications
Work EnvironmentPharmaceutical companies, CROs, or clinical trial sites managing inventory and logisticsClinical trial sites, hospitals, or research organizations coordinating trial activities
Employer & Industry UsageUsed in pharmaceutical and biotech industries to manage drug suppliesUsed in clinical research organizations and healthcare settings to oversee trial operations

While both roles support clinical research, Clinical Supply focuses on managing the logistics and inventory of trial materials, whereas a Clinical Trial Coordinator oversees the overall conduct and coordination of clinical trials. Understanding these differences helps in choosing the right career path or job search focus.

More about Clinical Supply jobs

What cities are hiring for Clinical Supply jobs?

Cities with the most Clinical Supply job openings:

What are the most commonly searched types of Clinical Supply jobs?

The most popular types of Clinical Supply jobs are:

What states have the most Clinical Supply jobs?

States with the most job openings for Clinical Supply jobs include:

What job categories do people searching Clinical Supply jobs look for?

The top searched job categories for Clinical Supply jobs are:

Clinical Supply jobs near you
Infographic showing various Clinical Supply job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $72,002 per year, or $34.6 per hour.

Executive Director, Clinical Supply Chain

Revolution Medicines

Redwood City, CA • Hybrid

$222K - $252K/yr

Full-time

Re-posted 22 days ago

Job description

The Opportunity:

The Executive Director, Clinical Supply Chain provides strategic leadership and operational oversight for end-to-end clinical supply chain activities across the organization.

Strategic Leadership

  • Define and execute the global clinical supply chain strategy aligned with the company's clinical development pipeline and long-term business goals.

  • Establishes strategies and processes to ensure uninterrupted supply for Revolution Medicines portfolio across all phases of development.

  • Lead and serve as subject matter expert for clinical supply chain planning, risk management, and execution of clinical supply chain activities.

  • Build scalable processes and infrastructure to support early- through late-phase clinical programs.

  • Strategic Planning on comparator sourcing management to ensure timely, compliant and cost-effective product availability.

  • Effective management of clinical studies executed in conjunction with collaboration partners.

  • Identify and implement overall clinical supply chain best practices.

Clinical Supply Operations

  • Oversee end-to-end clinical supply activities, including demand forecasting, protocol reviews, packaging, labeling, distribution, and returns.

  • Ensure uninterrupted supply of investigational medicinal products (IMP), including RevMed and comparator products.

  • Champions monthly Development Operations planning (DnOP) process in collaboration with PDM and Clinical Operation team members.

  • Ensures efficient global clinical supply chain distribution networks are in place.

  • Oversee comparator products demand and supply planning with expert level knowledge in comparator drugs and co-medications sourcing strategy

Cross-Functional Collaboration

  • Partner with Clinical Operations and Clinical Study Execution Teams (CSET) in study planning and execution.

  • Collaborate with PDM, Quality, and Regulatory to ensure compliant manufacturing, labeling, and distribution

  • Work closely with Finance on budgeting, forecasting, and cost optimization.

  • Work effectively with internal and external partners to develop sound strategies, identify and mitigate risks, and resolve issues as they arise.

Compliance & Quality

  • Ensure all clinical supply activities comply with GxP, ICH, FDA, EMA, and global regulatory requirements.

  • Expert knowledge of applicable GxP requirements and applicable regulatory guidances.

  • Lead inspection readiness activities as required for global filings and maintain and inspection ready organization.

Team Leadership

  • Build, lead, and mentor a high-performing clinical supply chain organization. Drives for excellence in execution of agreed upon strategies.

  • Establish clear performance metrics, development plans, and succession planning.

  • Foster a culture of accountability, continuous improvement, and collaboration.

  • Drives excellence in setting clear and actionable team goals.

Required Skills, Experience and Education:

  • Bachelor's degree in Supply Chain, Business, Engineering or Life Sciences with 20+ years of experience in pharmaceutical supply chain. Master's degree (MS, MBA) with at least 18 years of experience in pharmaceutical/biotech supply chain.

  • CPIM/CSCP certifications a plus.

  • At least 5 years of experience in a leadership/supervisory role.

  • Strong knowledge and experience with cGMP operations for small molecules, end- to end supply chain and demand/supply planning.

  • Effective vendor management and oversight skills

  • Excellent cross-functional leadership skills with effective communication skills.

Preferred Skills:

  • Proven leadership experience hiring, managing and developing teams.

  • Knowledge and experience with outsourced manufacturing operations. (CMO's)

  • Effective, open and transparent communication skills (verbal and written). Strong analytical, communication and executive level reporting skills.

  • Capable of working on multiple projects/tasks and able to meet timelines.

  • Self-starter with a high-level of comfort with ambiguity and complexity and the ability to multi-task while consistently delivering quality results.

  • Team-oriented, progressive thinker who enjoys participating in an innovative and creative work environment. 

    #LI-Hybrid  #LI-GL1

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