Associate Director, Clinical Supply Chain Planning Specialist
hace 3 semanas
Company Overview
CRISPR Therapeutics is a pioneering biotechnology company that has transformed the field of gene editing. With a diverse portfolio of product candidates across various disease areas, the company is committed to creating a new class of potentially transformative medicines. To accelerate its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies, including Bayer and Vertex Pharmaceuticals.
Position Summary
The Associate Director of Clinical Supply Planning will play a critical role in managing and optimizing global supplies to ensure timely availability of clinical supplies for clinical trials. This is a key position that will also be involved in setting up a robust clinical supply planning model to support clinical trials, ensuring alignment with company goals.
Responsibilities
Accountable for generating and maintaining a clinical supply plan to drive manufacturing, labeling, and forecasting supply activities across internal and external stakeholders. Lead and manage the supply planning for finished goods, drug product, drug substance, and critical components across multiple clinical programs. Collaborate with clinical teams and other internal/external stakeholders to forecast demand based on trial protocols and timelines.
Key Qualifications
Minimum 10-12+ years' experience working within a cGMP supply chain environment and/or with GCP regulations. Excellent computer skills (Microsoft Office Word, Excel, Outlook) required. Experience with clinical supply chain planning. Willingness to work in a flexible environment. Excellent organizational skills, enough to multi-task in an extremely fast-paced environment with changing priorities while maintaining attention to detail.
Preferred Qualifications
Experience with cold chain, and cell and gene therapies highly preferred. Additional specific qualifications in the area of clinical supply chain planning including APICS CPIM or CSCP, and related professional certifications.
Company Culture
CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility with the benefits of in-person interactions. Our employees work at least three days on-site, creating a collaborative work environment, where we cultivate mentorship opportunities, increase cross-functional communication, and offer opportunities for our employees to connect.
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