What are the responsibilities and job description for the Global Clinical Supply Manager position at Meet Life Sciences?
Job Summary
The Global Clinical Supply Manager supports global clinical trials by developing dosing plans, pharmacy manuals, and protocol-related drug administration content. This role ensures accurate IMP formulation, proper site guidance, and timely global supply availability. As a core member of cross-functional project teams, this position collaborates closely with Clinical Operations, CMC, Quality, Regulatory, CROs, and clinical sites to drive clinical supply strategy, execution, and compliance.
Responsibilities
- Develop pharmacy manuals, dosing schedules, and protocol sections related to drug preparation and administration.
- Partner with CMC on IMP packaging, labeling, distribution, and contract manufacturing activities.
- Build and maintain IMP supply plans based on study forecasts; ensure timely global availability.
- Manage IRT/IVRS setup, drug return processes, and vendor oversight.
- Oversee global clinical supply inventory, reconciliation, and real-time forecasting.
- Support clinical sites, caregivers, and patients on supply handling, storage, and returns.
- Monitor supply milestones, communicate timelines, and manage deviations, CAPAs, and change controls.
- Represent Clinical Supplies on project teams and contribute to cross-functional planning and process improvements.
Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, or related field; PharmD preferred.
- 5 years of clinical supply or investigational drug services experience (biotech preferred).
- Experience with global inventory management, forecasting, vendor oversight, and IRT/IXRS systems.
- Ability to review batch records and understand cGMP and IMP regulatory requirements.
- Ability to manage multiple priorities, meet tight timelines, and collaborate effectively across teams.