CrawlJobs Logo
AbCellera Biologics Logo AbCellera Biologics · Research and Development

Clinical Supply Chain Manager

Canada, Vancouver 124560.00 - 155700.00 CAD / Year · Job Posted January 18, 2026
Apply Position
Job Link Share

Job Description

Responsible for the end-to-end management of Investigational Medicinal Product (IMP) and ancillary supplies for global clinical trials. Ensuring the right product is in the right place, at the right time, and in the right condition for our clinical studies and patients. A strong collaborator who will work extensively with cross-functional teams, including Clinical Operations, CMC, Quality Assurance and Regulatory Affairs, as well as manage external partners (CMOs, depots and couriers) to execute flawless clinical supply strategies.

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

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

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
AbCellera Biologics - 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

Clinical Supply Chain Manager

8 matching positions

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

Senior Supply Chain Technician - Clinical Supply Chain - FT - Day

Functions as specialist, knowledgeable in Perioperative inventory, providing pur...
Location
Location
United States , Irvine
Salary
Salary:
24.76 - 32.66 USD / Hour
ucihealth.org Logo
UCI Health
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Must have 3 years prior job-related experience managing a multiple product inventory (SKU) and stock procurement system
  • Must be available to work overtime, weekends, and a rotating schedule to meet operational needs
  • Must be able to perform heavy manual tasks
  • Must be able to perform basic mathematical calculations
  • Must be able to effectively communicate, read, write and follow verbal and written instructions in English
  • Ability to manage multiple concurrent projects and maintain a work pace appropriate to the workload
Job Responsibility
Job Responsibility
  • Functions as specialist, knowledgeable in Perioperative inventory, providing purchasing and inventory management support to the main Operating Room (OR) and the Outpatient Surgical Suite (OSS)
  • Will build working relationships with vendors and product suppliers and seek opportunities for cost reduction
  • Will ensure the quality/accuracy of financial coding and tracking for expenditures
  • Duties also include maintaining PAR levels, ensuring the availability of supplies when needed, data entry of purchase requisitions, and follow-up on open requisitions and orders
  • Major emphasis is given to providing excellent customer service and meeting the requirements of the clinical staff in the OR and OSS
What we offer
What we offer
  • Medical insurance
  • Sick and vacation time
  • Retirement savings plans
  • Access to a number of discounts and perks
  • Fulltime
Read More
Arrow Right

Manager, Clinical Supply Chain

Proclinical is seeking a Manager, Clinical Supply Chain to oversee and execute c...
Location
Location
United States , Cambridge
Salary
Salary:
Not provided
proclinical.com Logo
Proclinical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a scientific field, Supply Chain Management, or a related discipline
  • Hands-on experience in global clinical supply chain management, including packaging, labeling, inventory, and distribution
  • Strong understanding of clinical trial operations and the drug development lifecycle
  • Foundational knowledge of GMP, GxP, GCP, and global regulatory requirements (e.g., FDA, EU)
  • Proficiency with systems and tools such as IRT/IXRS, inventory systems, Excel, Smartsheet, and ERP platforms
  • Expertise in risk identification, assessment, and mitigation strategies
  • Experience managing multiple studies/programs and overseeing vendors, CMOs, and CROs
  • Budget tracking, cost control, and financial oversight of clinical protocols
  • Strong problem-solving and decision-making skills with a risk-based approach
  • Proficient in MS Office tools, including Excel, PowerPoint, Visio, and Project
Job Responsibility
Job Responsibility
  • Manage end-to-end clinical supply chain activities, including IRT, packaging, labeling, distribution, inventory management, returns, destruction, and study closeout
  • Ensure timely and complete achievement of protocol milestones, such as FPI, SIV readiness, and on-time site/patient deliveries
  • Collaborate with Clinical Operations, QA, Regulatory, and CMOs to ensure efficient and compliant execution
  • Identify, escalate, and mitigate risks related to delays, deviations, and supply disruptions
  • Oversee temperature excursions and supply deviations, ensuring proper documentation and resolution
  • Maintain compliance and inspection readiness across all execution activities
  • Monitor inventory levels and supply availability across programs
  • Contribute to process improvements, tools, and ways of working within the clinical supply chain
  • Train and mentor other trial leads to enhance team capabilities
Read More
Arrow Right

Senior Manager Clinical Supply Chain

The Senior Manager, Clinical Supply Chain is a senior leadership role accountabl...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s or master’s degree in supply chain management, Engineering, Life Sciences, or Business Administration
  • advanced degree preferred
  • 12+ years of progressive experience in supply chain, planning, or operations roles within the pharmaceutical or biotechnology industry
  • Deep understanding of GMP and GCP interfaces, regulatory requirements, and the complexities of managing investigational products
  • Proven success leading large, cross-functional organizations within a global, matrixed environment
  • Strong digital and systems acumen, with experience implementing or operating platforms such as SAP, Anaplan, or equivalent
  • Demonstrated expertise in end-to-end clinical supply chain management, planning, vendor management, and business performance management
  • Exceptional analytical, strategic thinking, and communication skills, with a proven ability to influence senior leaders and drive enterprise outcomes
Job Responsibility
Job Responsibility
  • Lead the Development Supply Chain execution team, with end-to-end accountability for clinical material demand execution, packaging order conversion, and global distribution
  • Provide strong people leadership and operational governance while driving continuous improvement across inventory management, purchase order execution, NPI readiness, and compliant execution of temperature-controlled and specialty shipping requirements
  • Execute clinical trial readiness, including master data, artwork, and documentation management, ensuring GMP-compliant execution across all clinical programs
  • Provide leadership oversight for change controls, deviations, and CAPAs, driving standardization, training, and inspection readiness across the clinical supply chain organization
  • Lead material master data initiation, order management, and execution support for clinical manufacturing and packaging operations
  • Ensure continuous manufacturing and packaging support through process order management, 24/7 material availability, and optimization of inventory and order execution efficiency
  • Lead clinical logistics and cold chain operations, including logistics service provider vendor management, depot network planning, and compliant shipping lane design
  • Oversee clinical customer service and distribution quality activities, including proof-of-receipt monitoring, temperature data review, investigational product reconciliation, and resolution of distribution-related quality events and service complaints
Read More
Arrow Right

Manager Clinical Supply Chain

In this vital role, you will serve as Manager Clinical Supply Chain leading a te...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s Degree and 8+ years of supply chain, logistics, planning, or operations experience
  • OR Master’s Degree and 8+ years of relevant experience
  • Experience in regulated manufacturing or life sciences industry preferred
  • Experience managing people required
  • Strong experience in supply chain planning, procurement, and material management
  • Demonstrated success in people leadership, driving accountability, results, and growth of a team
  • Experience in regulated environments, preferably in pharmaceutical or biotechnology industries
  • Hands-on knowledge of SAP or similar ERP systems for material planning and management
  • Excellent communication skills, including fluency in English both in oral and written communication
  • Strong problem solving and analytical skills towards driving robust decision making
Job Responsibility
Job Responsibility
  • Lead and develop a team of 5 Senior Associates across Clinical Finish Drug Product planning and Non-Amgen Medicinal Product procurement
  • Define clear priorities, performance expectations, coaching, goals, and career development
  • Ensure effective staffing, resource management, and succession planning to maintain operational success
  • Foster a culture of accountability, compliance, and customer focus
  • Drive adoption of new technologies and AI to increase team productivity and enhance performance
  • Oversee production order conversion, stock transfer order initiation, and clinical planning cycle facilitation to ensure product supply plans are executed against appropriately, including infrequent rush execution during off-hours for global operations
  • Ensure success in study close out activities including material destruction
  • Oversee setup, procurement and inventory management for Non-Amgen Medicinal Products
  • Coordinate issue triage, corrective actions, and workload prioritization with global peers
  • Provide guidance on complex operational matters
  • 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

Supply Chain Manager For Clinical Trial Medications

In this role you will project manage the design, plan, and set-up of the study s...
Location
Location
Sweden , Mölndal
Salary
Salary:
Not provided
https://www.randstad.com Logo
Randstad
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Masters or equivalent
  • fast learner
  • self-driven
  • comfortable working in a high pace R&D environment
  • collaborative team player
  • flexible
  • strong communication, planning and problem-solving skills
  • strong influencing, negotiating and problem-solving skills across geographical and cultural boundaries
  • ability to adapt and operate in bespoke multiple systems
Job Responsibility
Job Responsibility
  • Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply
  • Ensure effective communication with project teams and key partners across a global network
  • Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies
  • Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction
  • Manage the Interactive Response Technology (IRT) system to execute demand and supply planning
  • Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls
What we offer
What we offer
  • competitive salary
  • benefits
  • collective agreements
  • large network
  • many social activities
  • Fulltime
Read More
Arrow Right

Clinical Supply Chain Logistics Manager

Talentmark is recruiting for a Clinical Supply Chain Logistics manager to join a...
Location
Location
United Kingdom , Moreton, Wirral
Salary
Salary:
34.00 GBP / Hour
ckgroup.co.uk Logo
CK Group
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree (or equivalent) in Supply Chain, Life Sciences, Engineering, or a related field
  • Proven experience in clinical supply chain logistics operations, preferably in a global clinical trial environment
  • Strong hands-on experience with STO management, shipment execution, and issue resolution
  • Demonstrated ability to operate effectively in high-pressure, time-critical (hyper-care) environments
  • Excellent communication skills with the ability to interface across study teams, regions, and external partners
  • Strong organizational skills, attention to detail, and ability to manage multiple priorities simultaneously
  • Experience working with external partners (e.g., CMOs, depots, logistics providers) is strongly preferred
Job Responsibility
Job Responsibility
  • Provide day-to-day operational oversight of all logistics activities for assigned clinical supply programs, ensuring delivery of IMP
  • Act as the single point of contact (SPOC) for logistics-related activities for designated studies, working with Study Teams, Regional Delivery Leads (RDLs), Trial Supply Managers (TSMs), and external partners
  • Provide weekly status reporting, including STO health, shipment execution, risks, mitigations, and prioritization
  • Fulltime
Read More
Arrow Right