We are seeking a Manager, Trial Supplies Management to create and maintain supply strategies for all investigational product based on the scientific and regulatory confines of the drug’s development. The ideal candidate will have a strong knowledge of the global drug development process, global regulatory requirements, and be able to collaborate with internal and external teams to ensure optimal use and alignment with study and corporate goals.
Requirements
- Collaborate with internal Global Clinical Supply Chain (GCSC) teams and external Customers and Service Providers
- Proactively define, plan, and communicate the clinical supply chain strategy
- Generate and drive strategies for continuous improvement
- Influence clinical and development timelines, study design and country selection
- Review and provide input to draft clinical protocols
- Communicate timelines and investigational product strategies to study and cross-functional teams
- Develop supply forecasts for complex studies
- Monitor inventory and analyze drug utilization versus forecast
- Issue Manufacturing and Packaging/Labeling requests to Clinical Supply Operations
- Monitor use date of investigational drug product for assigned protocols
- Support use date extension activities
- Ensure timely delivery of quality clinical supplies for all assigned compounds and protocols
- Participate in internal Trial Supply Management and Clinical Supply Chain meetings
- Collaborate with Clinical Supply Strategic Sourcing team to procure commercial drug
- Act as the main Clinical Supplies contact person for the assigned compound and associated studies
Benefits
- Health Coverage
- Wellbeing Support
- Financial Well-being and Protection
- Paid Time Off
- Flexible time off
- 11 paid national holidays
- 160 hours annual paid vacation for new hires
- Unlimited paid sick time
- Up to 2 paid volunteer days per year
- Summer hours flexibility
- Leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs