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Our staff also enjoy these benefits: Health, dental, vision, prescription drug and life insurance 401(k) retirement plan Paid time off and paid holidays Professional development assistance Career advancement opportunities MTC is proud to operate the Edison Job Corps Center in Edison, NJ where our staff provide quality services to our local youth.
$90,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The position will provide regulatory affairs strategic leadership for the company and novel drug development programs. 10+ years industry experience a must with RA novel drug development.
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A minimum of 8 years in clinical practice with outcomes research experience, or 5 years experience in drug development or related discipline in the field of biotechnology or real-world evidence.
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This position is responsible for providing strategic program leadership, technical expertise, and project management in the scale-up, development, commercialization, and transfer of medical devices and combination products, with a focus on autoinjectors, prefilled syringes, and other drug delivery systems.
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Minimum 6 years of solid and proven industry experience in pharmacovigilance and drug safety, both for Medicinal Products under development and marketed Medicinal Products. In depth understanding of good pharmacovigilance practices (GVP) Modules and current drug safety/pharmacovigilance regulations.
$250,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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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.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Deep knowledge of drug development, pharmacokinetics and pharmacology principles required. The Quantitative Pharmacology and Pharmacometrics (QP2) department drives model-informed drug discovery and development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions.
$285,800 a yearFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Our client – a Contract Development and Manufacturing Organization (CDMO) focused on drug discovery, development, and optimization – is seeking a highly qualified candidate to serve as Manager / Director of GMP Kilo Lab Operations in at their central NJ location.
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The Associate Scientific Director will be an engineering lead or project leader for drug candidates across all stages of development. Fluency in synthetic chemistry, small molecule drug substance process development, scale-up, and manufacturing.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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The Associate Director, Sr. Clinical Research Scientist (CS) in Clinical Development is an important role in the company supporting the development and life cycle of drug development projects.
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Areas of expertise include genomics, epigenetics, drug resistance, stem cell biology, drug discovery, diagnostics and biomarker development, and pharmacology. The Director, Life Science Commercialization is a pivotal role that provides leadership in the development and execution of commercialization strategies for life science based technology and solutions.
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We cover all key steps in the drug discovery and drug development value chain. We are looking for a Director of Sales/ Business Development for the North Americas region.
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Knowledge of Global Labeling Guidances, Drug Development and Commercialization of prescription medicines. A understanding of pharmaceutical drug development. Proven ability to understand regulatory implications of product strategy related to labeling development, assessment and management.
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Ensures that the labeling strategy is aligned with the overall product regulatory, registration, commercial and development strategy. Drive the labeling strategy to early development activities to ensure consideration of labeling in claims development programs.
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ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy (CGT), vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers.
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drug development jobs Title: director in Edison, NJ
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