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Employment with Sunrise is conditioned on completing and passing a drug test (which does not include marijuana), participating in testing requirements (e.g. Tuberculosis Test, Physical Evaluation.
$21 - $24.15 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Almac is an exceptional, award winning, drug development solutions provider at the forefront of the pharmaceutical industry. Professional development programs/ continuous learning opportunities.
$20.5 - $21.57 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Ability to pass a national criminal background check, motor vehicle record check & drug screening. Learning and Development Opportunities (we typically offer advancement within the first 6 months.
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Experience with protein drug product manufacturing processes and development (e.g., solution in vial/PFS, or lyophilization); container/closure assessment & selection, drug delivery (e.g., combination product, device & administration kit) feasibility and compatibility evaluation.
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As a Biopharmaceutical Drug Product, Principal Scientist/ Investigator, you will join the GSK sterile Drug Product Development organization and work on developing late phase drug product formulation, manufacturing process and delivery systems for protein-based therapeutics and NCEs.
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Provide leadership role in conducting multiple Phase I-IV clinical research trials across all functional areas of the drug development process. 10+ years of relevant industry experience in clinical/medical research or biotech/pharma; Vaccine product development expertise preferred.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Certara accelerates medicines using proprietary biosimulation software, technology and services to transform traditional drug discovery and development. Build relationships with stakeholders to support business development and project success.
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Doctoral degree (PhD., ScD or DrPH) in epidemiology or a relevant discipline (i.e. health services research, health outcomes research, public health, statistics or pharmaceutical sciences) OR Clinical degree (e.g., in medicine, pharmacy, nursing) or a masters degree in Epidemiology with 5+ years experience leading pharmaco-epidemiologic research in a drug development environment.
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At UBC, we provide services to enhance the entire drug development process and commercialization lifecycle - From clinical trial support to real-world evidence generation. At UBC, we provide services to enhance the entire drug development process and commercialization lifecycle - From clinical trial support to real-world evidence generation.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Application Scientist will support and lead method development using novel PWR technology, in a variety of applications, including drug discovery, protein interaction, and etc. Support and lead method development using novel PWR technology, in a variety of applications, including drug discovery, protein interaction, and etc.
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General understanding of drug development and pharmaceutical manufacturing from concept to launch, including requirements for product development, manufacturing, and marketing. Assist in the development and preparation of CMC submission documentation.
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In this role you will partner with project teams across the preclinical and clinical development portfolio, integrating drug development across all functions, and translating strategy into execution to deliver medicines to patients.
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Ensure that CDMOs activities and process development activities address drug product needs for pre-clinical testing, stability, and clinical trials. Compile, review, and archive data files related to drug product activities for early and late-stage development programs, including but not limited to protocols, reports, SOPs, engineering and cGMP records, stability, and supportive documentation, etc.
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The US Process Analytics group part of the GSK Research and Development division, is responsible for developing mechanistic, data-driven, and hybrid models to support the design and development of pharmaceuticals and biopharmaceuticals for both drug substance and drug product.
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In short, to be the partner of choice in drug development. As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.
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drug development jobs in Norristown, PA
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