Supervisor, Supply Chain Planning

Biogen - Cambridge, MA

Full-time - Mid Level

Hybrid - Cambridge, MA

Chemical Manufacturing

About the position

The Lead, Clinical Supply Management plays a crucial role in the supply management team, orchestrating the journey of clinical trial materials from conception to delivery. This position focuses on demand forecasting, meticulous planning, and precise execution to ensure that clinical trials are well-supported and aligned with the company's broader business strategy. The role involves engaging with various stakeholders, managing logistics, and contributing to the efficiency of the supply chain, particularly in the fields of neurology and rare diseases.

Responsibilities

• Engage in comprehensive demand analysis for clinical trials to develop supply forecasts.
• Coordinate with Clinical Operations and R&D to understand study specifics and requirements.
• Work closely with the Clinical Asset Planner to consolidate demand and inform supply strategies.
• Manage the logistics of international and US clinical trial material distribution, ensuring timely delivery to sites.
• Participate in supply management team meetings, contributing to and executing supply plans.
• Participate in vendor audits.
• Identify and implement process improvements for enhanced supply chain efficiency.
• Develop and maintain manufacturing and inventory plans based on trial demands.
• Monitor and report on progress against manufacturing plans, highlighting any supply risks.
• Recommend and enact corrective actions to achieve inventory targets and mitigate supply risks.
• Contribute to new product launches, clinical studies, and supply chain projects.
• Support integrative projects across functions, streamlining processes and systems.

Requirements

• Bachelor's degree with a minimum of 3 years of supply chain experience.
• Proven analytical and problem-solving abilities, with a track record of generating innovative solutions.
• Strong relationship management skills, with experience liaising with 3rd party logistics providers, CMOs, and/or various internal groups.
• Excellent communication skills, capable of conveying complex plans, risks, and contingencies across diverse teams.

Nice-to-haves

• Experience within a regulated environment, such as biotech/pharmaceutical, medical devices, or food industries.
• Experience within a cGMP supply chain and familiarity with GCP regulations; clinical supply experience.

Benefits

• Opportunities for learning and growth.
• A commitment to building a culture of inclusion and belonging.
• A pioneering spirit within a mid-sized biotechnology company.