1

Clinical Supply Manager Jobs (NOW HIRING)

Clinical Supplies Manager II

Alameda, CA · On-site

$132K - $188K/yr

Lead effort for clinical supply management functionality. * Monitor and manage clinical supply activities through IRT from study start-up through study closure. * Proactively drive the labeling ...

Clinical Supplies Manager II

Alameda, CA · On-site

$132K - $188K/yr

Lead effort for clinical supply management functionality. * Monitor and manage clinical supply activities through IRT from study start-up through study closure. * Proactively drive the labeling ...

Clinical Supply Chain Director

Alameda, CA · On-site

$164.50 - $234.50/hr

They develop clinical supply chain strategies to ensure availability of supply through development ... Manage procurement of comparator drug products and matching placebo as required; prepare manuals ...

This individual will manage vendors (e.g., shipping and logistics vendors, clinical supply depots and Interactive Response Technology (IRT) vendors) from study start-up through close-out. This role ...

This individual will manage vendors (e.g., shipping and logistics vendors, clinical supply depots and Interactive Response Technology (IRT) vendors) from study start-up through close-out. This role ...

Clinical Supplies Manager

Princeton, NJ · On-site

$80K - $120K/yr

The Clinical Supplies Manager is responsible for overseeing the planning, procurement, packaging ... Forecast supply needs based on enrollment projections and protocol requirements. * Coordinate with ...

Position Overview The Manager, Clinical Supply Operations,is responsible formeeting Immunome's supply requirements by enabling and overseeing cGMP operations performed at Contract Development and ...

New

Showing results 41-60

Clinical Supply Manager information

See salary details

$63.5K

$106.2K

$164.5K

How much do clinical supply manager jobs pay per year?

As of Sep 3, 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 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 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 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.

More about Clinical Supply Manager jobs

What cities are hiring for Clinical Supply Manager jobs?

Cities with the most Clinical Supply Manager job openings:

Who are the top companies hiring for Clinical Supply Manager jobs?

The top employers for Clinical Supply Manager jobs are:

What states have the most Clinical Supply Manager jobs?

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

Infographic showing various Clinical Supply Manager job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $106,193 per year, or $51.1 per hour.

Clinical Supplies Manager II

Exelixis

Alameda, CA • On-site

$132K - $188K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 12 days ago


Job description

SUMMARY/JOB PURPOSE:

The Clinical Supplies Manager II oversees all aspects of clinical supply management including packaging, labeling, monitor inventory levels, and distribution by interacting with internal and external supply partners/vendors to ensure supply of IMP are sufficient at depots and clinical sites.

Essential Duties And Responsibilities:

  • Lead effort for clinical supply management functionality.
  • Monitor and manage clinical supply activities through IRT from study start-up through study closure.
  • Proactively drive the labeling, packaging, release, distribution of clinical supplies at external CMO's for assigned studies, ensuring the project timeline is met or exceeded.
  • Ensure domestic and global distribution arrangements are in place with external vendors to allow shipment following availability of technical and regulatory releases.
  • In collaboration with relevant partners, create forecasts and packaging design based on study needs to ensure optimized supply plan.
  • Partner with key stakeholders (including Quality Assurance and Regulatory Affairs) to ensure supplies are labelled and released for clinical site shipment for global clinical trials.
  • Work cross-functionally to develop IRT to develop specifications and perform UAT.
  • Design and/or review label text to meet product requirements and ensure compliance with US and international regulations.
  • Represent clinical supplies function at clinical trial team meetings; communicate plan and timelines to internal and external customers and partners.
  • Work with cross-functional teams to develop specifications and user testing of IRT systems provided by 3rd party vendors.
  • Ensure appropriate system documentation is transferred to TMF and ready for inspection readiness.
  • Utilize appropriate software and IT systems to effectively manage key project activities.

Supervisory Responsibilities:

  • None

EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:

Education/Experience:

  • BS/BA degree in related discipline and a minimum of seven years of related experience; or,
  • MS/MA degree in related discipline and a minimum of five years of related experience; or,
  • Equivalent combination of education and experience.
  • Certification in assigned areas is a plus.

Experience/The Ideal for Successful Entry into Job:

  • Demonstrated experience with clinical supply management planning, labeling, packaging, and distribution.
  • Clinical Supply management experience using contract manufacturing companies strongly preferred.
  • Working knowledge and experience with Interactive Response Technologies (IRT) such as IVRS and IWRS

Knowledge/Skills:

  • Willingness to work in a fast paced, evolving environment.
  • Knowledge of GMP batch record development, review, and approval processes.
  • Knowledge of Interactive Voice/Web response systems for use in clinical studies.
  • Working knowledge of regulations relating to clinical labeling, packaging and distribution activities.
  • Working knowledge of GMP/GCP/GLP regulations required.
  • Excellent project management and communication skills.

JOB COMPLEXITY:

  • Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors.
  • Uses professional concepts and company objectives to resolve moderate to complex issues in creative and effective ways.
  • May also work on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors.
  • Exercises judgment in selecting methods, techniques and evaluation criteria for obtaining results.
  • Networks with key contacts outside own area of expertise.

Working Conditions:

  • 20% travel to vendor sites, team meetings, and/or other offices.

Work Environment/Physical Demands:

Our office is a modern, open-plan space that foster collaborations and creativity. Teams work closely together, sharing ideas and solutions in a supportive atmosphere. We provide all necessary equipment, including dual monitors and ergonomic chairs, to ensure a comfortable workspace.

#LI-MB1

Our compensation reflects the cost of labor across severalU.S. geographic markets, and we pay differently based on those defined markets. The base pay range for this positionis $132,500 - $188,000 annually. The base pay range may take into account the candidate's geographic region, which will adjust the pay depending on the specific work location. The base pay offered will take into account the candidate's geographic region, job-related knowledge, skills, experience and internal equity, among other factors.In addition to the base salary, as part of our Total Rewards program, Exelixis offers comprehensive employee benefits package, including a 401k plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Employees are also eligible for a discretionary annual bonus program, or if field sales staff, a sales-based incentive plan. Exelixis also offers employees the opportunity to purchase company stock, and receive long-term incentives, 15 accrued vacation days in their first year, 17 paid holidays including a company-wide winter shutdown in December, and up to 10 sick days throughout the calendar year.

If you have a disability and need an accommodation in relation to the recruiting process, please email us at: ApplicantAccommodations@exelixis.com.


WORKING CONDITIONS:

Our office is a modern space that fosters collaboration and creativity. Teams work closely together, sharing ideas and solutions in a supportive atmosphere. We provide all necessary equipment, including dual monitors and ergonomic chairs, to ensure a comfortable workspace.


DISCLAIMER:
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.


We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.