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Sr Specialist, Clinical Supply Management
As Biogen’s portfolio expands and our Clinical Drug Supply operation continues to grow, we are seeking experienced staff to forecast, coordinate and manage investigational medicinal supplies for global study protocols.
The Sr Specialist, Clinical Supply Management, is responsible for study drug supply per assigned protocols serving global patient populations in varied therapeutic areas across Biogen’s neurology and rare disease portfolio. Key job responsibilities are overseeing daily supply chain activities in global markets while serving internal and external customers. This position requires a high level of organizational skills, ability to work well independently and balance a diverse workload.
Accountable for availability and distribution of finished goods per protocol
Drive finished good packaging strategy
Develop manufacturing/inventory plan based on demand
Routinely identify and communicate any supply risks to management and supporting teams
Participate in vendor audits
Analyze cross-functional processes, identify and implement improvements
Support new hire training
Engage in cross-functional projects such as process improvements and system implementations or enhancement
Serve as the single point of contact per protocol to internal and external stakeholders
Initiate and maintain import licenses
Manage deviations and quality events
Co-develop IRT supply strategy
Analytical/Problem Solving - Draws from past experiences to develop solutions to problems that require a high degree of ingenuity, creativity, and innovativeness. Identifies and escalates issues as necessary.
Relationship Management – Routine contact with external 3rd party logistics providers, CMOs, and other internal functional groups. Track order, delivery and invoicing throughout the supply chain. Provide routine updates and identifies/communicates issues to managers and customers.
Communication - Excellent written and verbal skills, ability to communicate plans, risks and contingencies across various functional groups.
Technical - Experience working within a cGMP supply chain environment and with GCP regulations desired. Minimum 2 years working within the biotech/pharmaceutical, medical devices, food, or other regulated environment.
Bachelor of Science or Bachelor of Arts required
Supply chain background, clinical science or healthcare background preferred
Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients’ lives and on changing the course of medicine. Together, we pioneer. Together, we thrive.