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Collaborate with cross functional teams including but not limited to Medicinal Chemistry, DMPK, Toxicology, QA, Analytical Development, Process R&D, Project Management and Regulatory to timely achieve project goals.
$160,000 - $200,000 a yearExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Global Discovery and Development Sciences (GDDS) Boston, part of the US R&D hub, is building a new siRNA Nonclinical Development department with cross-functional scientific expertise, including toxicology, safety pharmacology, PKPD, ADME, outsourcing management, and non-clinical project management.
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The Principal Toxicologist will be responsible for the design and execution of nonclinical development toxicology studies conducted externally, interpretation and communication of the toxicology data/reports to support drug development decisions, and for summarizing and writing regulatory submissions.
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The Associate Director, Portfolio Management Insights, Portfolio & Strategic Operations (P&SO), drives portfolio management insights development and delivery to the Global Program Teams (GPTs), Therapeutics Areas (TAs) leaders, Hematology Oncology Cell Therapy (HOCT)/Immunology Cardiovascular Neuroscience (ICN) leadership, crucial for strategic decision-making within the drug development portfolio.
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Analytical Skill, Analytical Skill, Analytical Thinking, Chemical Biology, Chemistry, Clinical Trials, Collaboration, Communication Skills, Curiosity, Data, Data Analysis, Design Of Experiments, Detail-Oriented, Drug Development, Drug Discovery, Ethics, Gene Therapy, Immunology, Inventory Management, Laboratory, Lifesciences, Machine Learning (Ml), Management, Medical Research, Molecular Biology {+ 10 more.
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Contribute to the Biomedical Research drug discovery process with the goal of progressing the development of new therapeutic options for patients with chronic kidney diseases. Design and execute in vitro and in vivo research plans to deliver high quality data-driven package and enable project decisions.
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We are seeking an experienced and highly motivated Director/Senior Director, Drug Product/Formulation Development who will report to the VP of CMC. This individual will drive the drug product development and strategy including pre-formulation, formulation, scale-up and manufacture for all our preclinical and clinical projects.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Collaborate with internal and external CMC functions including project management, chemical development, analytical development, and supply chain to align priorities and project timelines.
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Knowledge in project management and CMC regulatory requirements. Oversight of GMP drug product manufacturing, late-stage development based on Quality by Design (QbD) and Design of Experiments (DoE), and drug product process validation/commercialization.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Strong track record in drug product development, CDMO management, and largescale manufacturing. Build relationships and lead outsourced drug product development and manufacturing activities including contracts, timelines, and budgets a to meet overall project timelines.
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The selected candidate will manage integrated drug development projects across the full scope of the development paradigm and ensure projects are delivered on time, budget, and with high quality using proven project management decision support tools and strong leadership skills.
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The Project Director (PD) leads and manages the project and is accountable for project deliverables and results, with full accountability and necessary authority for the development, implementation, and monitoring of the project, including (1) vision and strategy; (2) project management and financial oversight; (3) documentation and communication; (4) client(s) and stakeholder(s) relationships; and (5) coordination and synergy with other MSH and USAID projects.
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Referred to as GRAD-TB, the project is designed to scale up and improve management of drug -resistant ( DR - TB ) in USAID - supported countries and focus on expanding access to high quality treatment services.
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The MEL Director will lead development and implementation of a strong MEL plan consistent with the USAID results framework, coordinate the collection of data including conducting field visits for data validation, monitor the quality and completeness of data sets, contribute to the development of the program and document project performance against established outputs and indicators.
$116,000 - $165,900 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Adhere to MSH procurement integrity and institutional standards and procedures in all project management responsibilities. Provide regularly updated reports on the status of implementation against the project goals and objectives to the Project Director, USAID, and other program managers as required.
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project management drug development jobs Title: drug
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