Clinical Supply Chain Planning Director
1 month ago
CRISPR Therapeutics is seeking an experienced Associate Director of Clinical Supply Chain to join our team. This role will be responsible for managing and optimizing global supplies to ensure timely availability of clinical supplies for clinical trials.
Key Responsibilities- Generate and maintain 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.
- Coordinate with manufacturing sites, clinical sites, and label/storage/distribution vendors and other internal stakeholders to ensure consistent inventory is available at each node to sustain the clinical trial(s).
- Define and implement KPIs/metrics related to supply and demand.
- Work closely and proactively with internal/external stakeholders to ensure seamless operation of clinical trials and address any challenges.
- Bachelor's degree in Biological Sciences or related field.
- 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.
- Clear and succinct verbal and written communication skills.
- Strong analytical, problem-solving, and critical thinking skills.
- Ability to influence others and work independently and in a team environment.
- 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.
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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