Clinical Distribution Lead
Offre en anglaisManage end-to-end clinical distribution and on-time delivery of investigational products to global depots and clinical sites. Collaborate with cross-functional teams to resolve operational issues and drive process improvement initiatives within a GMP-compliant environment.
- Hybride
- Mississauga, ON
- Publié 19 août 2026
- Postuler avant le 18 sept. 2026
- 1 poste
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Résumé du poste
We are looking for a Clinical Distribution Lead to join our Global Clinical Supply Chain team. This role is responsible for managing end-to-end clinical distribution activities for a portfolio of global clinical trials, ensuring the timely and compliant delivery of investigational products to depots and clinical sites worldwide. The successful candidate will collaborate with cross-functional teams to support a diverse pipeline of clinical studies while maintaining high standards of quality, efficiency, and patient focus. Work Location: Mississauga, Hybrid (Only 3 days onsite per week) Key Responsibilities Manage on-time delivery performance for network supply shipments to meet study requirements and patient demand Actively participate and engage on Protocol Execution Teams (PETs), Global Supply Execution Teams (gSETs), and ad-hoc distribution-related meetings Drive resolution of operational and system issues impacting on-time delivery, collaborating with internal and external providers Execute and coordinate network depot supply in coordination with the Clinical Demand and Supply Leader and other partners as needed Lead and participate in cross-functional and internal distribution-related projects and process improvement initiatives supporting global distribution strategy Execute with the highest level of accuracy within the CLARA system, performing 1st- and 2nd-level diagnostics Operate within a GMP-compliant environment, ensuring adherence to established quality procedures Process event records, including quality incidents, CAPAs, and Changes (Planned Events), as applicable Requirements Degree (BA, BS, MS, or MBA) in Business (Operations Management or Supply Chain Management), Biotechnology, or a related field 2–4 years of experience in Clinical Trial Management, logistics, warehouse management, or another Supply Chain discipline, preferably within the Biotechnology or Pharmaceutical industry Strong knowledge of and experience with SAP / ERP systems Experience working within cross-functional, cross-cultural, and agile organizational models APICS and/or SCOR certification is a plus Operational Excellence, Six Sigma, or Lean training is a plus Mindset and Behaviors Action-oriented, with the ability to influence internal and external stakeholders Demonstrates curiosity, active listening, and a willingness to experiment and test new ideas, with a focus on continuous learning and improvement Collaborative, agile mindset with a genuine interest in contributing to cross-functional teams and self-directed team organization Able to solve problems and manage complex situations autonomously Comfortable managing multiple tasks and priorities simultaneously Expected Compensation Range: 65K The final compensation offered will be determined based on the candidate’s level of experience, skills, and qualifications, in compliance with applicable pay transparency requirements. Canadian Experience Requirement: No Canadian work experience is required for this position. Candidates are encouraged to apply regardless of previous Canadian experience. Artificial Intelligence (AI) Disclosure: No Artificial Intelligence (AI) tools are used in the screening, assessment, or selection of candidates for this position. All stages of the recruitment process are conducted by human recruiters and hiring managers. Statement Regarding Job Vacancy: This position is a Job creation, created to support ongoing project needs. Recruitment Process & Feedback Timeline: Candidates will receive feedback on their application within a maximum of 45 days from the date of application or from their most recent interview stage. Why choose us An international community bringing together more than 110 different nationalities An environment where trust is central: 70% of our leaders started their careers at the entry level A strong training system with our internal Academy and more than 250 modules available A dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.) Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.
Ce que vous ferez
Manage end-to-end clinical distribution and on-time delivery of investigational products to global depots and clinical sites. Collaborate with cross-functional teams to resolve operational issues and drive process improvement initiatives within a GMP-compliant environment.
Exigences
Requires a degree in Business, Biotechnology, or a related field with 2-4 years of experience in clinical trial logistics or supply chain. Proficiency in SAP/ERP systems and experience in pharmaceutical or biotech industries are essential.
Avantages
• Internal Academy with 250+ modules • Internal events (afterworks, team buildings)
Compétences indiquées
- Gestion de la chaîne d’approvisionnementSouhaitée
- LogistiqueSouhaitée
Autres compétences pertinentes
Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.
- Clinical Distribution
- Supply Chain Management
- SAP
- ERP Systems
- GMP Compliance
- Logistics
- Warehouse Management
- Clinical Trial Management
- Process Improvement
- Cross-functional Collaboration
- CAPA
- Six Sigma
- Lean
- Operational Excellence
- CLARA System
- Stakeholder Management
Domaines d’emploi
- Logistics
- Healthcare
- Management & Leadership
- Consulting
- Science & Research
Renseignements supplémentaires
- Formation minimale
- Baccalauréat
- Expérience minimale
- 2+ ans
- Postuler avant le
- 18 sept. 2026
- Langue de l’offre
- anglais
- Heures de travail
- 40 heures par semaine
- Présence au bureau
- 3 jours par semaine
- Niveau d’expérience
- Mid-Senior level
- Mode de candidature
- La candidature directe est offerte