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The QC Director is responsible for all activities supported by the site QC Analytical Testing Laboratory in a CDMO that provides GMP ADC Manufacturing capability to the Biopharmaceuticals industry.
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As an Associate Director, Biostatistician, you will be a champion of Otsuka’s culture and values and will be responsible for providing statistical expertise/input in the drug development, including clinical development plan and regulatory submission strategy.
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The Role: Director of Data Science – NLP, LLM and GenAI. The Team: S&P is a leader in risk management solutions leveraging automation and AI/ML. This role is a unique opportunity for an experienced ML scientist and hands-on NLP/Gen AI/ LLM senior scientist to grow into the next step in their career journey and apply her or his domain expertise in NLP, deep learning, GenAI, and LLMs to drive business value for multiple stakeholders while mentoring and growing a ML Data Science team.
$225,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Associate Director, Regulatory Operations role is accountable for managing regulatory submission related activities, providing business ownership and management of IT systems within the scope of Regulatory Affairs/Operations.
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Revolution Field Strategies (RFS) is seeking talented, driven individuals for the role of Regional Organizing Director (ROD) who will be responsible for building, managing, and leading regional teams for canvassing, voter registration, and signature collection projects.
$78,000 a yearFull-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Collaborate with Membership Director on programmatic elements designed to engage and grow member engagement. This person will report to the Chief Audience Officer and utilizing current research and best practices, the Director of Education & Engagement will move the institution forward with a mixture of educational, wellness, teambuilding, performance and community engagement and more.
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We are looking for Product Quality Leader, Director. Provide product quality oversight and strategic input over product and analytical development, characterization, tech transfer, comparability, and validation studies conducted for designated products in collaboration with PD, MSAT, AD, and QC (including Stability.
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Responsible for the oversight of Translational Medicine preclinical safety assessment/toxicology deliverables, with a clear understanding of functional interdependencies and critical path activities.
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The Director of Events is responsible for Lumen's presence at trade shows, destination events, internal townhalls, internal/external streaming events, board meetings, and more. Lumen Director of Events Trenton, New Jersey Apply Now Lumen connects the world.
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Job Description: Title: Director, Content Licensing Market Data Management Reports To: Global Content Licensing Director Department: Partners & Licensing. Specifically, the Director, Content Licensing Market Data Management will work in partnership with the Market Date Operations, Market Data Engineering, Dow Jones Business Units, Procurement and critical market data vendors to foster alignment between Dow Jones's business unit needs and vendor products, services, and activities.
$175,000 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Data Science Solutions: development and application of advanced analytical methods inclusive of Artificial Inteligence (e.g. Machine Learning, Deep Learning, NLP, Voice Recognition, RPA, etc
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Pharmacy Director Responsibilities Overview: Lead and oversee clinical and business functions of the Pharmacy and Infusion center including both the compounding and in-office dispensing aspects of the center.
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Provides personal arrangements and compositions for the choir to match their capabilities.
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Director, Medical Safety Assessment Physician (Immunology) Assist the Medical Safety Assessment (MSA) TA Head/Lead in developing and maintaining state-of-the-art Pharmacovigilance (PV) processes and procedures within BMS Drug Development and WWPS.
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The Executive Director, Clinical Development & Quality Operations is a critical management position within the R&D Quality organization that is responsible for the development and strategic oversight of the Therapeutic Area Quality, Vendor and Data Quality as well as Quality Risk Management.
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Title: director Company: Novartis Suchergebnisse in Ewing, NJ
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