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Freeport-McMoRan promotes a drug/alcohol-free work environment using mandatory pre-employment drug testing and on-going drug and alcohol testing, as allowed by applicable laws. Freeport-McMoRan promotes a drug/alcohol free work environment through the use of mandatory pre-employment drug testing and on-going random drug testing as per applicable State Laws.
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Some attractions in Leadville include the National Mining Hall of Fame and Museum, Ski Cooper, Tennessee Pass Cookhouse, Tabor Opera House and the Leadville National Fish Hatchery. Please be advised that Freeport-McMoRan will never request payment for job-related expenses from applicants.
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Must include day-to-day hands-on experience with analytical methods such as HPLC / UPLC and GC, MS, dissolution, compendial, spectroscopy, KF, DSC, TGA, and working knowledge of microbiological methods such as MLT, endotoxins, sterility, etc., required to control and monitor sterile and oral drug products.
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MD with 10+ years of experience in drug development and drug safety/pharmacovigilance, with specific expertise in clinical oncology, immunology, or genetics. Job Overview: This position is well-suited for a Medical Director with substantial expertise in drug development and safety, providing a unique opportunity to strategize the implementation of safety surveillance for clinical trials, oversee the management of safety signals, take charge of cross-functional teams, and contribute to the development of regulatory safety deliverables.
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Freeport-McMoRan promotes a drug/alcohol-free work environment through the use of mandatory pre-employment drug testing and on-going random drug testing as allowed by applicable State laws.
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Dive into the dynamic world of AI and Digital Technologies at Genmab The Role: As an Associate Digital Product Manager in IT & Digital, you will have a critical role in overseeing the product strategy, development/implementation and management of technology products in different focus areas in Global Drug Safety and Pharmacovigilance.
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Areas of expertise include genomics, epigenetics, drug resistance, stem cell biology, drug discovery, diagnostics and biomarker development, and pharmacology. The Bioinformatician Fellow will work under the supervision of the Bioinformatician and support multiple labs.
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Understand the scientific principles required for manufacturing AAV drug substances and products, including cell culture, bioreactor operation, vector production and aseptic processes. Upstream Bioprocess - Technical Services/Manufacturing Scientist (TS/MS) role is responsible for providing technical support for the development, implementation, and technical transfer of compliant manufacturing of gene therapy drug substance and drug product for clinical and commercial manufacture.
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Expertise in medicinal chemistry principles, cheminformatics, ADME, ML/AI and structure-based drug discovery. Expert proficiency in one or more commercial drug discovery platform such as ICM, Schrodinger, CCG and/or OpenEye.
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Our Client's global life sciences practice, one of the largest in the U.S., is seeking a regulatory counsel with at least 10+ years of industry experience in drug/biologics development to join our FDA regulatory group.
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Drives and implements the Oncology Research strategy in a particular area of research in concordance with the overall Oncology precision drug development strategy; The Oncology Research Portfolio Lead will have global responsibility to drive strategy in target identification to contribute to a competitive and sustainable early research portfolio and deliver preclinical candidates in Oncology as defined by the Oncology precision drug development strategy in select areas of research.
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This position has been classified as a safety sensitive position and is subject to our drug testing policy to include pre-employment, random, reasonable suspicion and post-accident for the following prohibited substances: marijuana, amphetamines, opioids, phencyclidine (PCP), and cocaine, as well as any drug not approved for medical use by the U.S. Drug Enforcement Administration or the U.S. Food and Drug Administration.
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Reporting to the Prior Authorization Supervisor , the Clinical Authorization Specialist is responsible for managing all work related to molecular pathology, high-cost drug, and off-label drug authorizations.
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The drug product team is also investing in building new platforms to support complex formulations such as lipid nanoparticles, Antibody Drug Conjugates and AAV and other non-viral vector delivery.
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Current working knowledge of cellular and molecular immunology, cell biology, or related discipline, with an applied understanding of antibodies and antibody generation, biologics drug discovery research and disease target evaluation.
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drug job Title: post doctoral fellow Company: Emory University
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