Who We Are:
Zura is a clinical‐stage biotechnology company advancing clinical development of novel therapeutic candidates for autoimmune and inflammatory diseases with significant unmet medical need. Our work is focused on understanding immune‐mediated disease and translating that science into carefully designed clinical programs, with patients and their challenges guiding our approach.
Zura is building and advancing a growing portfolio of clinical programs informed by strong scientific expertise and disciplined execution. Across the organization, teams work closely together to progress development thoughtfully, with a shared emphasis on data quality, rigor, and integrity.
At Zura, we operate as One Zura. This means collaborating across functions, valuing diverse perspectives, and taking shared ownership of our work—from problem‐solving to execution. Joining Zura means contributing to patient‐focused clinical development in a hands‐on environment where individual effort matters, collaboration is expected, and people are encouraged to grow while working toward a common goal.
What You'll Do:
The Clinical Trial Supply Chain Manager is responsible for overseeing the supply chain and logistics of clinical trial materials to ensure timely and efficient delivery to sites across the globe. This role involves collaboration with internal teams, external vendors, and clinical sites to manage inventory, forecast supply needs, and ensure compliance with regulatory requirements.
Responsibilities:
* Develop and manage clinical trial supply plans to meet project timelines and requirements.
* Coordinate with vendors and internal teams to ensure the timely production, packaging, labeling, and distribution of clinical trial materials
* Monitor inventory levels and implement strategies to mitigate risks of shortages or overstock.
* Oversee the logistics and distribution processes to ensure efficient and compliant delivery of trial supplies to clinical sites.
* Manage relationships with logistics providers and ensure adherence to service level agreements.
* Resolve any issues related to shipping, customs, and site delivery.
* Ensure all clinical trial supplies are compliant with regulatory requirements and guidelines.
* Maintain accurate and up-to-date documentation for all supply chain activities.
* Participate in audits and inspections as required.
* Collaborate with internal teams to forecast supply needs based on trial enrollment and protocol requirements.
* Serve as the point of contact within study teams for clinical trial supply-related matters.
* Communicate effectively with internal and external stakeholders to provide updates on supply status and address any issues.
* Conduct regular meetings with project teams to review supply chain progress and challenges.
* Identify opportunities for process improvements and implement best practices in clinical trial supply management.
* Stay updated on industry trends and advancements in clinical trial supply chain management.
Required Qualifications:
* 3+ years of experience in clinical trial supply management or a similar role within the pharmaceutical or biotech industry.
* Strong knowledge of GCP (Good Clinical Practice), GMP (Good Manufacturing Practice), and regulatory requirements for clinical trials.
* Proven experience in managing global supply chains and working with international logistics providers.
* Excellent project management and organizational skills.
* Strong communication and interpersonal skills with the ability to work effectively in a remote team environment.
* Proficiency in supply chain management software and tools.
Education:
* Bachelor's degree in Supply Chain Management, Logistics, Life Sciences, or a related field.