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Sourcing Strategy Development - Co-develop and implement sourcing strategies with the business unit to enable development and commercialization of cell and gene therapy products.
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Job DescriptionDirector, R&D Quality, GCP - Cell Gene Therapy (CGT)The Director of R&D Quality, GCP - Cell Gene Therapy (CGT) reports directly to the Head of RDQA and is a trusted advisor and partner to clinical and quality stakeholders and business partners and supports the program and study level quality leads in key quality related clinical activities and deliverables for all CGT programs across the Vertex clinical portfolio.
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The Director of R&D Quality, GCP - Cell Gene Therapy (CGT) reports directly to the Head of RDQA and is a trusted advisor and partner to clinical and quality stakeholders and business partners and supports the program and study level quality leads in key quality related clinical activities and deliverables for all CGT programs across the Vertex clinical portfolio.
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This client is a growing international full-service CDMO/CRO within the biotechnology space looking to aggressively expand its footprint in the US. The company has a strong base of API/Small Molecule, Biologics, Clinical Research, Bioanalytical Sciences, DMPK, Cell and Gene Therapy and other capability centers across the US. This business has developed a fantastic brand in the US through exceptional service which drives repeat business.
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Associate Director, BaseCamp Business Development ElevateBio is a technology-driven cell and gene therapy company, accelerating access to the cutting-edge technologies and expertise to change the future of medicine.
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Providing advice on regulatory issues for both marketed and pipeline products; actively collaborates with management, Global Regulatory Lead and cross functional colleagues within Alexion (i.e., commercial, research, clinical development, medical affairs, business development, legal, manufacturing, quality, portfolio management, financial, human resources, etc.
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Lead development and execution of the commercial and business strategy in the Cell Therapy Franchise. Acts as day to day commercial and business escalation for Cell Therapy within RESILIENCE, serves active role in governance of customer relationships and site on respective PAD and manufacturing SLT (s.
$235,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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We are now recruiting a Director, Clinical Regulatory Writing (CReW), Immunology Cell Therapy Program Lead. In this role you will provide expert leadership to the delivery of the product pipeline through partnering with senior leaders to define and lead the global communications strategy.
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The Director Project Controls plays a strategic leadership role with relentless focus on Business Development and organizational growth while ensuring Project Delivery via their own billability, as well as, training, mentoring, and coaching their teams in both the evolution and continued operational excellence of Precision for Medicine's Manufacturing Solutions practice area.
$200,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Experience 8+ years of experience in a strategic consulting firm or corporate development team in a large corporation for new business development in advanced therapy, biotech, or healthcare related industries, including experience leading project ideation, scoping, strategic planning, strategic partnership development, M&A activities, deal structuring, and post-deal integration processes.
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Experience in cell and gene therapy. Strong knowledge of US drug development and regulatory policy; excellent scientific and business judgment. Monitoring the development of new regulatory requirements or guidance documents and advising product teams of the impact on the business or development programs.
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