CrawlJobs Logo
BioMarin Pharmaceutical Logo BioMarin Pharmaceutical · Logistics

Intern, clinical supply chain

United States 24.00 - 32.00 USD / Hour · Job Posted March 01, 2026
Apply Position
Job Link Share

Job Description

The Intern will support key operational, documentation, reconciliation, and reporting activities across the Clinical Supply Chain (CSC) organization. This internship provides hands on exposure to clinical trial execution, supply chain operations, health authority documentation practices, contract and financial tracking, and the application of AI-enabled tools to streamline and enhance CSC processes.

Job Responsibility

  • Documentation Repository & eTMF Support
  • CMO Contract Reconciliation & Dashboard Optimization
  • Investigational Product (IP) Reconciliation for Study Close Out
  • Enhancement of CSC Metrics & Reporting
  • AI-Enabled Tool Development & Automation Concepts

Requirements

  • Currently pursuing a bachelor’s or master’s degree in supply chain, Business Operations, Engineering, Industrial Engineering, Human Resources, or a related field
  • Must be available to work full time, 40 hours a week
  • Must be currently enrolled as a full-time student at an accredited U.S. based university or college and enrolled in the fall term after the completion of the internship OR have graduated within 1 year of the start of the program
  • Must be able to relocate if necessary and work at the designated site for the duration of the internship for on-site, hybrid roles
  • Some positions will be open to remote interns, but employee must be within United States borders

Nice to have

  • Interest in clinical supply chain operations, clinical trials, documentation systems (eTMF), and regulated environments
  • Knowledge of or interest in learning contract structures, spend tracking, and supply‑related financial concepts
  • Experience with Power BI, Tableau, or similar data visualization tools is a plus
  • Exposure to AI tools or automation concepts (prompt engineering, workflow design, NLP) is beneficial
  • Curiosity, proactive mindset, and interest in process improvement and digital enablement

What we offer

  • Paid hourly wage, paid company holidays, and sick time
  • Apply skills and knowledge learned in the classroom to on-the-job experiences
  • Comprehensive, value-added project(s)
  • Develop skills specific to your major
  • Opportunities for professional development by building relationships and learning about other parts of the business
  • Participate in company all hands meetings, monthly community lunches
  • Corporate office amenities such as: 24/7 on-site gym, coffee truck, snacks
  • Access to Employee Resource Groups
BioMarin Pharmaceutical - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Intern, clinical supply chain

8 matching positions

Senior Associate Clinical Supply Chain – Global Clinical Customer Service (GCCS)

Reporting to the Manager, Development Supply Chain, you will support the global ...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s Degree & 4+ years of supply chain, logistics, pharmaceutical operations, or related experience
  • OR Bachelor’s Degree & 5+ years of supply chain, logistics, pharmaceutical operations, or related experience
  • OR Associate’s Degree & 8+ years of relevant experience
  • OR High School Diploma / GED & 10+ years of relevant experience
  • Experience in clinical supply chain, pharmaceutical operations, or regulated operational environments
  • Strong problem-solving, issue resolution, and analytical skills
  • Ability to work effectively in a global, matrixed environment
  • Strong service-oriented mindset, responsiveness, and stakeholder support skills
Job Responsibility
Job Responsibility
  • Manage and resolve distribution complaints related to investigational product shipments supporting global clinical trials
  • Intake and triage Category-1 inquiries from clinical sites, study teams, and internal stakeholders
  • Coordinate cross-functional issue resolution and escalate risks appropriately
  • Review temperature data for investigational product shipments delivered to clinical trial sites
  • Perform temperature excursion assessments within Quality Management Systems following established procedures
  • Partner with Quality and study teams to support investigations, disposition decisions, and inventory status updates
  • Maintain accurate, complete, and inspection-ready documentation
  • Support study-level reconciliation activities to ensure accurate investigational product accountability
  • Manage investigational product returns in accordance with procedures and regulatory requirements
  • Support intake, documentation, and coordination of investigational product complaints
  • Fulltime
Read More
Arrow Right

Senior Associate Clinical Supply Chain – Global Clinical Customer Service (GCCS)

Reporting to the Manager, Development Supply Chain, you will support the global ...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master's Degree & 4+ years of supply chain, logistics, pharmaceutical operations, or related experience
  • OR Bachelor's Degree & 5+ years of supply chain, logistics, pharmaceutical operations, or related experience
  • OR Associate's Degree & 8+ years of relevant experience
  • OR High School Diploma / GED & 10+ years of relevant experience
  • Experience in clinical supply chain, pharmaceutical operations, or regulated operational environments
  • Strong problem-solving, issue resolution, and analytical skills
  • Ability to work effectively in a global, matrixed environment
  • Strong service-oriented mindset, responsiveness, and stakeholder support skills
Job Responsibility
Job Responsibility
  • Manage and resolve distribution complaints related to investigational product shipments supporting global clinical trials
  • Intake and triage Category-1 inquiries from clinical sites, study teams, and internal stakeholders
  • Coordinate cross-functional issue resolution and escalate risks appropriately
  • Review temperature data for investigational product shipments delivered to clinical trial sites
  • Perform temperature excursion assessments within Quality Management Systems following established procedures
  • Partner with Quality and study teams to support investigations, disposition decisions, and inventory status updates
  • Maintain accurate, complete, and inspection-ready documentation
  • Support study-level reconciliation activities to ensure accurate investigational product accountability
  • Manage investigational product returns in accordance with procedures and regulatory requirements
  • Support intake, documentation, and coordination of investigational product complaints
Read More
Arrow Right

Senior Associate Clinical Supply Chain – Global Clinical Customer Service

Reporting to the Manager, Development Supply Chain, you will support the global ...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master's Degree & 4+ years of supply chain, logistics, pharmaceutical operations, or related experience OR Bachelor's Degree & 5+ years of supply chain, logistics, pharmaceutical operations, or related experience OR Associate's Degree & 8+ years of relevant experience OR High School Diploma / GED & 10+ years of relevant experience
  • Experience in clinical supply chain, pharmaceutical operations, or regulated operational environments
  • Strong problem-solving, issue resolution, and analytical skills
  • Ability to work effectively in a global, matrixed environment
  • Strong service-oriented mindset, responsiveness, and stakeholder support skills
Job Responsibility
Job Responsibility
  • Manage and resolve distribution complaints related to investigational product shipments supporting global clinical trials
  • Intake and triage Category-1 inquiries from clinical sites, study teams, and internal stakeholders
  • Coordinate cross-functional issue resolution and escalate risks appropriately
  • Review temperature data for investigational product shipments delivered to clinical trial sites
  • Perform temperature excursion assessments within Quality Management Systems following established procedures
  • Partner with Quality and study teams to support investigations, disposition decisions, and inventory status updates
  • Maintain accurate, complete, and inspection-ready documentation
  • Support study-level reconciliation activities to ensure accurate investigational product accountability
  • Manage investigational product returns in accordance with procedures and regulatory requirements
  • Support intake, documentation, and coordination of investigational product complaints
  • Fulltime
Read More
Arrow Right

Supply Chain Manager – Development Supply Chain Technologies

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...
Location
Location
United States , Thousand Oaks
Salary
Salary:
105010.70 - 142073.30 USD / Year
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate or master’s degree and 2 years of SAP or IS system experience
  • OR Bachelor’s degree and 4 years of SAP or IS system experience
  • OR Associate’s degree and 8 years of SAP or IS system experience
  • OR High school diploma / GED and 10 years of SAP or IS system experience
Job Responsibility
Job Responsibility
  • Manage assigned end-to-end processes and ensure their readiness for execution of clinical supply chain processes
  • Partner with DTI to assist with the resolution of technical incidents utilizing the Integrated Service Management-ServiceNow (ISM-SN) application
  • Troubleshoot technical incidents with end users utilizing both internal resources and outside organizations such as External Trial Operations (ETO)
  • Monitor iDoc failures and determine the root cause of issues
  • Act as a change record owner to support continuous improvement initiatives
  • Manage documentation and maintenance of clinical customization requirements to support readiness for key projects, audits, and inspections
  • Manage audit readiness playbooks for assigned processes
  • Interpret customers’ needs to identify potential opportunities for improvements
  • Support development of business cases for proposed system enhancements
  • Support and/or lead enhancement implementation
What we offer
What we offer
  • Health and welfare plans for staff and eligible dependents
  • Financial plans with opportunities to save towards retirement or other goals
  • Work/life balance
  • Career development opportunities
  • Retirement and Savings Plan with generous company contributions
  • Group medical, dental and vision coverage
  • Life and disability insurance
  • Flexible spending accounts
  • Discretionary annual bonus program
  • Stock-based long-term incentives
  • Fulltime
Read More
Arrow Right

Sr Associate Clinical Supply Chain Support Office

In this vital role, you will serve as Sr Associate, supporting the Design and Se...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 5+ Years of experience with Bachelors degree or equivalent in logistics, business administration or life science
  • Typically relevant working experience, preferably in the biotechnology or pharmaceutical industry
  • Typically relevant working experience in an international and regulated environment
  • Understanding of fundamentals of logistics/supply chain principles (especially BOM)
  • Experience in planning
  • Experience in project management techniques
  • Advanced experience in MS Office applications (Word, Excel)
  • Fluency in English, both in oral and written communication
  • High quality standards with regards to work
  • Ability to set priorities and timely escalation
Job Responsibility
Job Responsibility
  • Serve as Sr Associate, supporting the Design and Setup of the Clinical Supply Chain
  • Managing master data requests for product materials, Bill of Materials (BOM), and study related attributes in SAP
  • Creation of the Clinical Artwork requests and facilitating prioritization of outstanding attributes in relation to the request form
  • Creation and maintenance of Product Specification Files, and Depot Plans
  • Coordinate and prioritize artwork creation process via initiation and routing of clinical artwork creation request forms
  • Creates and maintains Product Specification File Study throughout the life cycle of the clinical trial
  • Creates and maintains third party depot plans and cross docks to support global study footprint
  • Maintains Metrics for Global Setup lead team
  • Contributes to monthly Workforce planning cycle
  • Fulltime
Read More
Arrow Right

Sr Associate Clinical Supply Chain Support Office

In this vital role, you will serve as Sr Associate, supporting the Design and Se...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 5 Years of experience with Bachelor degree or equivalent in logistics, business administration or life science
  • Typically relevant working experience, preferably in the biotechnology or pharmaceutical industry
  • Typically relevant working experience in an international and regulated environment
  • Understanding of fundamentals of logistics/supply chain principles (especially BOM)
  • Experience in planning
  • Experience in project management techniques
  • Advanced experience in MS Office applications (Word, Excel)
  • Fluency in English, both in oral and written communication
  • High quality standards with regards to work
  • Ability to set priorities and timely escalation
Job Responsibility
Job Responsibility
  • Master Data in ERP (SAP)
  • Initiate clinical label material requests
  • Requesting Finished Drug Product Materials, Bill of Materials (BOM), Work Breakdown Structure (WBS) elements, Custom Values and ensures timely availability to adhere to overall project timelines
  • Ensures setup of Study Design Tables
  • Coordinate and prioritize artwork creation process via initiation and routing of clinical artwork creation request forms, facilitating discussions to resolve issues and following up on outstanding queries
  • Creates and maintains Product Specification File Study throughout the life cycle of the clinical trial
  • Creates and maintains third party depot plans and cross docks to support global study footprint
  • Maintains Metrics for Global Setup lead team
  • Contributes to monthly Workforce planning cycle
  • Fulltime
Read More
Arrow Right

Clinical Supply Chain Manager - Change Control and Deviations

In this vital role, you will serve as the Manager Clinical Supply Chain, managin...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor degree or equivalent in logistics, business administration or life science
  • 5 year’s relevant working experience, preferably in the biotechnology or pharmaceutical industry
  • 5 year’s relevant working experience in an international and regulated environment
  • Advanced understanding of fundamentals of logistics principles
  • 3 year’s relevant working experience in project leadership and project management techniques
  • Advanced experience in MS Office applications
  • Fluency in English, both in oral and written communication
  • High quality standards with regards to work
  • Ability to set priorities and timely escalation
  • Strong communicating and facilitating issue resolution skills
Job Responsibility
Job Responsibility
  • Lead and develop team of 2 Senior Associates for Support Office Activities
  • Define goals, manage performance, and support career development
  • Ensure appropriate staffing, cross-training, and succession planning
  • Foster a culture of accountability, compliance, and customer focus
  • Drive adoption of new technologies and AI to increase team productivity and enhance performance
  • Owning and project managing Change Control Records related to Clinical Product Life Cycle changes, or clinical protocol amendments
  • Owning (major) deviation records
  • Owning Corrective Action/ Preventative Action (CAPA) records
  • Ensure efficient and compliant execution of assigned clinical supply chain processes with patient-centric mindset
  • Closely coordinate issue triage and workload prioritization with global peers
Read More
Arrow Right

Clinical Supply Chain Manager

Responsible for the end-to-end management of Investigational Medicinal Product (...
Location
Location
Canada , Vancouver
Salary
Salary:
124560.00 - 155700.00 CAD / Year
abcellera.com Logo
AbCellera Biologics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Demonstrated expertise in cGMP, GCP, and global clinical trial regulations (e.g., FDA, EMA)
  • Experience managing packaging, labeling, and distribution partners (CMOs and all external partner organizations)
  • Bachelor’s degree in a scientific discipline, Supply Chain Management, or a related field, plus 8+ years of relevant work experience in the pharmaceutical or biotechnology industry, with at least 3 years in a direct clinical supply chain role
  • Hands-on experience with Interactive Response Technology (IRT/IXRS) systems is essential
  • Proven ability to manage complex, temperature-controlled (cold chain) logistics
Job Responsibility
Job Responsibility
  • Developing and maintaining global supply plans for clinical trials, including demand planning forecasts across AbCellera’s programs
  • Managing and maintaining global inventory across all central depots and clinical sites, ensuring uninterrupted supply while utilizing ERP/inventory systems for accurate record keeping
  • Managing packaging, labelling, and distribution activities with CMO partners
  • Coordinating global shipments of clinical supplies, ensuring strict compliance with international trade regulations, import/export requirements, and customs documentation
  • Managing and qualifying temperature-controlled shipments (cold chain), collaborating with Quality Assurance to resolve any temperature excursions
  • Collaborating with teams and vendors to set up, manage and lead User Acceptance Testing (UAT) for Interactive Response Technology (IRT/IXRS) systems governing inventory, randomization, and drug assignment
  • Ensuring all clinical supply activities strictly adhere to Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and global regulations
  • Acting as the Clinical Supply Subject Matter Expert on clinical study teams, collaborating with CMC, Regulatory Affairs (label approvals/submission requirements), and Clinical Operations
  • Overseeing drug accountability, returns, and destruction, ensuring complete documentation, and assisting in the developing and managing of the clinical supply budget for assigned studies
What we offer
What we offer
  • Equity
  • Annual bonus dependent on team and company performance
  • 6% (non-match) RRSP contribution
  • CAD $1,500 annual Active Lifestyle Allowance
  • Annual vacation
  • Professional development opportunities
  • Comprehensive health benefits
  • Scientific and technical mentorship
  • Fulltime
Read More
Arrow Right