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Investigational Device Exception, though some non-significant risk studies are conducted with only IRB approval. Trials may be single or multi-site and could be investigator or industry sponsored. The Clinical
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proven track record developing creative and successful marketing strategies and campaigns; a passion for continued industry knowledge and trends is a must; strong listening skills in all meetings and pass
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cell-based therapies, working in a GMP-regulated facility. This role supports manufacturing activities from cell culture to product harvesting and cryopreservation, ensuring that high-quality cell
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Lead GMP Specialists, CGT Manufacturing, Laboratory Manager III Health Sciences Core Research Facilities - Pennsylvania-Pittsburgh - (25004389) Lead GMP Specialist, Cell and Gene Therapy Leads
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to sustain the University’s leadership in high-impact, federally and industry-supported clinical trials. The candidate should hold a medical degree or an advanced research degree in a related field, possess
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, including milestone, budget, and timeline management. Experience that spans a range of funders, including government, foundation, and industry. A history of the establishment of successful collaborations
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Junior Market Research Analyst Office of Industry and Economic Partnerships - Pennsylvania-Pittsburgh - (25005232) The Junior Market Research Analyst is an active member of the LifeX Due Diligence
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Junior Investment Analyst Office of Industry and Economic Partnerships - Pennsylvania-Pittsburgh - (25005233) The Junior Investment Analyst is an active member of the LifeX Due Diligence Investment
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Program Manager, Community Hub Office of Industry and Economic Partnerships - Pennsylvania-Pittsburgh - (25005242) The Program Manager for LifeX’s Community Hub efforts is responsible for creating
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that have garnered external funding and interactions with national and international academic and industry entities Experience in a large hospital-based hematopathology service and in molecular