Manager / Senior Manager Clinical Supply

Responsibilities:
- Support study set-up activities including protocol review, supply assumption development, and vendor kick-off coordination.
- Translate clinical supply plans into packaging and labeling specifications for execution with external CMOs and vendors.
- Assist with development and maintenance of study-level drug supply forecasts.
- Manage day-to-day supply operations including inventory monitoring, shipment coordination, and depot management.
- Monitor retest and expiry dates; coordinate resupply, relabeling, or destruction as needed.
- Coordinate with external packaging, labeling, and distribution vendors on deliverables and timelines.
- Support IRT/RTSM build, UAT, and ongoing configuration management.
- Provide clinical supply input to pharmacy manuals and investigational product reference materials.
- Represent clinical supply in cross-functional study team meetings.
- Ensure all activities comply with GCP, GMP, and applicable regulatory requirements.
- Maintain accurate documentation across supply systems, trackers, and SOPs.

Qualifications/Skills:
- Bachelor’s degree in supply chain management, logistics, pharmacy, or related fields.
- 5+ years of clinical supply chain or similar pharmaceutical/biotech industry experience.
- Proficiency with IRT/RTSM, ERP systems, and Microsoft Excel.
- Strong understanding of GxP/GCP and pharmaceutical supply chain operations.
- Excellent communication, proactive problem-solving, and project management.
- Key competencies: attention to detail, strategic forecasting, vendor relationship management, risk mitigation, strong interpersonal skills.
- 10% travel may be required.