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Responsibilities include establishment of, and adherence to, non-clinical study timelines, monitoring of study conduct at the TPO via communication with the Study Director and/or onsite observation, and real time communication with the Toxicology ADME/ToxPath/Drug Disposition (ATP) team throughout study planning, execution and reporting.
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Manage a team of Medicinal Chemistry research scientists within a collaborative environment to drive drug discovery process. Lead small molecule drug discovery programs and determine Medicinal Chemistry team direction to advance one or more projects.
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Conduct modeling and simulation to inform drug discovery and translation of drug properties. Our aim is to find the right dose of the right drug for the right patient, embodying the model-informed drug discovery and development (MIDD) paradigm.
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At Genentech Computational Sciences (gCS) Prescient Design, we are revolutionizing drug discovery with cutting-edge machine learning techniques. Participate in cutting-edge research in machine learning and methods development for scientific discovery, including large language models and drug discovery.
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Areas of expertise include genomics, epigenetics, drug resistance, stem cell biology, drug discovery, diagnostics and biomarker development, and pharmacology. The Center for Discovery and Innovation (CDI), was established by Hackensack Meridian Health (HMH) as an academic basic and translational research enterprise to rapidly translate science innovation to the clinic to improve outcomes for patients with cancer, infectious diseases, autoimmune disease and other acute and chronic diseases.
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You will be a key team member responsible for utilizing NextMAP TM , a NextRNA proprietary computation engine that identifies driving disease lncRNAs∯*∯ You will have an opportunity to work with a diverse team of bioinformaticians, biochemist, chemists, and biologist to support drug discovery programs for next wave of RNA therapeutics.
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We need someone who understands the purpose, components, and outcomes of successful drug development and safety assessment. At Lilly, we unite caring with discovery to make life better for people around the world.
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We are currently seeking an environmental scientist/toxicologist in the Environmental Health & Safety (EH&S) Department. Summary/ObjectiveThis early-career environmental scientist/toxicologist will join a collaborative team that supports our human health-based consulting services for a wide range of industrial and commercial clients.
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Drug Hunting Focus: The candidate is expected to exhibit strong problem-solving abilities and be familiar with understanding and resolving issues that lie at the interface of peptide discovery, peptide engineering, pharmaceutical developability and formulation, and biology.
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With a combination-focused pipeline that exploits the power of six scientific platforms (Immuno-Oncology, Tumor Drivers and Resistance, DNA Damage Response, Antibody-drug Conjugates, Cell Therapy and Epigenetics) to help address unmet clinical needs in a host of hematological cancers, we are motivated by a dedication to the scientific discovery and collaboration that will one day help eliminate cancer as a cause of death.
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Associate Director, Toxicology - Cell & Gene TherapyAre you a seasoned Toxicologist ready to influence the future of Cell & Gene Therapy (CGT)? Associate Director, Toxicology - Cell & Gene TherapyAre you a seasoned Toxicologist ready to influence the future of Cell & Gene Therapy (CGT.
$150,000 - $200,000ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Our team has created the industry's most advanced molecular AI platform called GEMS (Genesis Exploration of Molecular Space), to accelerate and optimize small molecule drug discovery and to enable the discovery of novel first-in-class and best-in-class small molecule drugs for challenging and/or undruggable targets.
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As a member of the small molecule drug discovery division, the successful candidate will leverage their advanced protein biochemistry skills to contribute to small molecule drug discovery programs and work collaboratively with cross-functional teams to further advance these innovative projects.
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Your New Chapter Awaits:As a Senior Study Director in the CGT department, you’ll play a pivotal role in advancing the science that keeps us all safe. Interface with different teams, including in vivo scientists, QC/QA, Account Managers/Sales, and the veterinary staff.
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Experience with GLP (Good Laboratory Practice) and non-GLP toxicology studies. Knowledge and experience in cell and gene therapy programs are preferred. Your Credentials: Ph. D. in Toxicology, Pharmacology, or a related field.
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