The Associate Supplier Governance role is responsible for managing end-to-end purchase-order activities for clinical-trial suppliers, ensuring compliance with company procurement and clinical trial requirements.
Requirements
- Bachelor’s / Master's degree (preferred: scientific degree or RN) or equivalent experience.
- 2 - 5 year experience in PO management, preferably within clinical research, CRO, biotech or pharmaceutical settings.
- Demonstrated experience with PO/SOW management and clinical supplier budgets.
- Experience working in a global matrix environment is preferred.
- Knowledge of Good Clinical Practice (GCP).
- Strong organizational and project management skills; able to manage competing priorities.
- Strong Proficiency with enterprise procurement/P2P workflows, Microsoft Office Word, Excel and SharePoint.
- Financial acumen sufficient for budgeting, forecasting and PO balance monitoring.
- Clear written and verbal communication; ability to coordinate cross-functional stakeholders.
- Problem-solving orientation and appropriate escalation judgment.
- Professional collaboration skills.