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The Biologics group is responsible for various functions criticalfor drug development such as: antibody discovery, molecular biology, cell line engineering,protein engineering, biophysical analytics, and functional cell assays.
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Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance.
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This influential and self-sufficient position will make significant contributions to drug discovery, preclinical studies, biomarker identification and development, and nonclinical research.
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A dynamic program manager with deep knowledge of the drug discovery and development process, including demonstrated experience with leading programs through preclinical development and regulatory submission, with a strong preference for early clinical development experience with biologics development and product candidates in immunology.
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Alongside ongoing clinical trials, SystImmune has a strong preclinical pipeline of potential cancer therapeutics in the discovery or IND-enabling stages, representing cutting-edge biologics development.
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Lead development and validation of Immunoassays, cell-based assays, and/or flow cytometry as required, to detect/monitor biologics in clinical and preclinical studies associated with drug development.
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The Senior Director ensures phase-appropriate assay development requirements as programs progress through the stages of biologics drug development with a line of site towards development of assays which will be robust, reproducible and capable of being qualified and validated for GMP use, for commercial products.
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BMS is looking for a Principal Scientist with a desire to contribute in the fast-paced early development matrix environment by supporting pre-formulation, physico-chemical characterization, and formulation development of oral and parenteral dosage forms for new drug candidates in support of preclinical and clinical studies.
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Annually, over 125 Labs use the facility across wide range of cutting-edge basic science and clinical translation research including tumor biology, imaging technology development, diagnostic and therapeutic drug development, neuroimaging, cardiovascular disease, neurobiology, and multi-modality imaging.
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Work cross functionally, leading or participating in matrix teams and integrating development with drug substance process development, commercial, preclinical, clinical, regulatory, supply chain and quality.
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Founded in 2004, Pharmaron has invested in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and CGT products.
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Subject matter authority in rheumatology, immunology and /or inflammatory bowel disease from drug development experience in non-oncology indications. Drug development experience in immunology indications strongly preferred (eg trials in diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis (RA) and/or inflammatory bowel disease.
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Founded in 2015, the company has built a portfolio of 20+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
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We are seeking a highly motivated Lab Research Coordinator to contribute to our pre-clinical and clinical research efforts as part of the Orthopaedic Translational Engineering Lab. In this role, you will support preclinical studies while actively engaging in the development and prototyping of cutting-edge medical devices.
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Must have an understanding of the preclinical research stage of drug development to properly support Investigational New Drug (IND) Enabling Programs of Lovelace Biomedicals Commercial Sponsors.
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