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Proven record leveraging computational biology to support drug discovery and development. 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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The incumbent will be responsible for drug screening, cell-based assay development, and biomarker discovery. Work at the bench to develop and execute established and Client molecular and cell-based assays for drug screening as well as understanding molecular pathways (Proliferation, Apoptosis, Flow Cytometry etc.
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You'll be responsible for designing, executing, and reporting on the analytical development of small molecule chemistry experiments, degradation pathways, characterization, and stabilization techniques for ophthalmic and injectable drug products.
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Expert knowledge of drug development strategies for various modalities including small molecules, biologics, therapeutic peptides, therapeutic areas (including neuroscience and endocrineology) and regulatory regions including US, Canada, Europe and Japan.
$200Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Design and execute in vitro and in vivo studies to facilitate drug discovery and platform development in various disease areas. Develop, validate, and perform assays to characterize ligand-receptor interactions and to gain mechanistic understanding of drug delivery.
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Candidates should have strong experience in a relevant scientific area, such as drug discovery, therapeutic development, computational chemistry, computer vision, statistics, artificial intelligence, modeling, simulations computational genomics or biology, statistical genetics, data science, chemistry, or biology.
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Exposure to AI/ML-driven drug discovery and development. iBio’s mission is to decrease drug failures, shorten drug development timelines, and open up new frontiers against the most promising targets.
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We focus on bringing client drug compounds from discovery to the clinic with services that include analytical development, pre-formulation testing, formulation development, GMP manufacturing and stability storage and testing as well as Clinical Supply Services.
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Documenting:DevSecOps CI/CD with GitLab Ultimate Provisioning tools including Terraform, Puppet, Ansible, or related frameworks Rancher Federal & RKE2 Highly available/fault tolerant solutions Software Development experience in Python, Java, C Cloud networking deployment (e.g. Software defined networking, Ingress, Egress.
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Establish strategies tailored to each development phase for small molecule drug products, select an appropriate drug delivery platform, and engage in manufacturing processes aligned with preclinical, clinical, and market image development requirements.
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The Senior Manager of Drug Safety & Pharmacovigilance (PV) Quality, is a key role and is responsible for oversight of Drug Safety & PV quality, compliance, and alliance management activities, thus always promoting inspection readiness and maintaining a robust global compliance program within the Quality Assurance department.
$150,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Department’s 18 divisions include Academic General Pediatrics, Child Development & Community Health; Allergy, Immunology, and Rheumatology; Cardiology; Dermatology; Dysmorphology; Emergency Medicine; Endocrinology; Gastroenterology; Genetics; Genome Information Sciences; Hospital Medicine; Infectious Diseases; Neonatology; Nephrology; Pharmacology & Drug Discovery; Rehabilitation Medicine; and Respiratory Medicine.
$25.75 - $30.72 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Rate of Pay: $130,000 per yearSchedule – Full Time, 8hr shifts, Monday – FridayOur staff also enjoy these benefits: Health, dental, vision, prescription drug and life insurance 401(k) retirement plan Short and long-term disability Paid time off and paid holidays Professional development assistance Career advancement opportunities MTC is proud to operate the San Diego Job Corps Center in Imperial, CA where our staff provide quality services to our local youth.
$130,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Global drug experience in oncology drug development. Reporting to the Senior Vice President of Clinical Development, theDirector, Global Study Lead (GSL) will be a key member of the Rakuten Medical Inc. (RMI) Clinical Operations Team. The GSL will function as the product team leader to plan, organize, and coordinate all operational aspects of a global multi-regional clinical study from protocol development through database lock while ensuring timelines for different regions are fulfilled.
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Directs and participates in the development and submission of clinical research protocols and other documentation to the Institutional Review Board (IRB), local human research protection program, sponsors, monitors, and/or Food and Drug Administration (FDA.
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drug development jobs in San Diego, CA
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