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Minimum 7 years of early clinical research and drug development experience, experience in translational and precision medicine research and biomarker sciences. Teva's R&D Global Early Clinical Development is hiring for a Senior Translational & Precision Medicine Leader (STPML) - Immunology in the Translational and Precision Medicine (TPM) group who will be accountable for the development and implementation of the overarching TPM strategy and deployment of innovative research approaches to enhance the probability of success of drug asset programs in the Immunology therapeutic areas (TA.
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Track record in drug discovery/development in large or small biotech/pharmaceutical companies, leading translational/biomarker studies or innovative efforts to deploy technologies and assays for enhanced translational capabilities or similar skill sets in academia.
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Combined we have over 20,000 multidisciplinary professionals worldwide collaborating daily to protect and conserve natural landscapes, create firm foundations for communities to stand on, and champion sustainable development to combat climate change.
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PSEG offers a unique experience to our more than 12,000 employees - we provide the resources and opportunities for career development that come with being a Fortune 500 company, as well as the attention, camaraderie and care for one another you might typically associate with a small business.
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Hybrid work arrangements will allow work from home combined with your presence on-site at our US HQ in Florham Park, NJ.Good knowledge of 21CFR11 and GCP.Good knowledge of Drug development process and BiostatisticsCurrent knowledge in technologies and tools related to Statistical programming or Biostatistics.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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For all roles, PSEG's drug and alcohol testing program includes pre-employment testing, testing for cause, and post-incident/accident testing. Please note that the use of CBD products may result in a positive drug test for THC/Marijuana and such use is not a legitimate medical explanation for such a positive result.
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Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations. Support study committee (e.g., DMC, Steering Committee, Advisory Board, etc) logistics and presentation development.
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Working understanding of medical concepts and some familiarity with safety activities in drug development and postmarking and global safety health authority requirements. Support individuals in aspects of project management, drug development and MST requirements, as appropriate to meet overall MST/subteam needs.
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Experience with CMC regulatory documents (IND/CTAs, BLA/NDAs, MAAs, responses, variations and briefing documents) Knowledge of FDA, EMA and/or ICH guidelines and CMC regulations Experience in drug development processes and post-approval requirements Experience in developing CMC regulatory strategy Experience in project management Have a solution-oriented approach to problem solving Ability to plan/prioritize work of group members and guide/develop others.
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Zebra is a federal contractor and is committed to an alcohol and drug free workplace. Support Research and Development activities, including participation in product/process development trials, carrying out new types of raw material and product characterization/performance testing and use of experimental materials.
$42,200 - $63,400 a yearExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The Senior Principal Scientist will collaborate across BMS sites with Analytical, Drug Product, Drug Substance, Quality, and Regulatory leads to execute drug product formulation/process development support, analytical strategies for drug product methods and specifications, analytical control strategies, and support of product development up to drug application submissions and approval.
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The Senior Principal Scientist role will be responsible for development and execution of drug and myeloma asset centric translational strategies in hematology for assigned programs. Translational Medicine Hematology at BMS has a long-standing history of scientific rigor as evidenced by our peer-reviewed publications, delivery of drug approvals including Revlimid, Pomalyst, Idhifa, Inrebic, Reblozyl, Vidaza and Onureg, strong academic collaborations and talent development.
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The Global Safety Physician will support the continued development of the Drug Safety and Pharmacovigilance (DSPV) organization. Knowledge of drug development process, safety monitoring and risk/benefit analysis in clinical trials.
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Pharmaceutical or related industry knowledge desired, including experience and understanding of drug development and life-cycle management in the regulated environment. The Manager, Statistics provides statistical expertise to support the research and development organization.
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Deep understanding of drug development process, international drug approval procedures and standards (e.g., ICH-E3, ICH-E6, eCTD) and industry-wide standards in clinical document management (e.g., DIA TMF reference model.
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drug development jobs in East Hanover, NJ
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