We are seeking an experienced and highly organized Clinical Trial Supply Manager to oversee the management and execution of clinical trial supplies from setup through to closeout. This role involves coordinating the timely delivery, packaging, distribution, and destruction of clinical trial supplies, ensuring compliance with regulatory standards and efficient processes throughout the trial lifecycle.
In this role, you will be responsible for collaborating with the Clinical Management and CMC teams to develop and implement comprehensive supply plans, manage supply risks, and handle the logistics of primary and secondary packaging. You will also manage the clinical trial distribution plan, ensuring efficient delivery with a focus on quality, cost, and timelines. Additionally, you will be responsible for preparing documentation for importation, managing the returns and destruction process, and ensuring timely closure of the Trial Master File (TMF) for each study.
As part of the Commercial Packaging team, you will contribute to the commercial packaging of the product, defining packaging requirements, managing relationships with packaging suppliers, and ensuring the regulatory approval of artwork and packaging. You will also be responsible for serialization and managing the application of serial numbers.
The ideal candidate will have a degree in life sciences and at least 3 years of experience in clinical trial supply or commercial packaging, with a solid understanding of international GMP, GDP, and GCP regulations. Strong communication, interpersonal skills, and a team-oriented approach are essential for success in this role.
This role is based in Basel and is fully on-site.
Job Title : Commercial Packaging and Clinical Trial Supplies Manager
If you're looking to contribute to a dynamic and fast-paced environment where your expertise in clinical trial supply management will make a real impact, we encourage you to apply.
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