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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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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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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 role provides statistical input into the drug development plan, researches and leads the statistical design, analysis, and reporting of clinical trials, and interacts with global regulatory agencies.
$250,800 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of drug development process and an understanding of how diagnostic development can shape drug development and commercialization is strongly preferred. Contributes to CDx project teams for the diagnostic, under the direction of the Global Program Teams (GPT) CDx representative for the therapeutic or under the guidance of the CDx portfolio leader, covering all areas from CDx assay development through CDx approval and launch.
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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.
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In addition, responsible for facilitating transition from drug development to commercial product. Provide leadership and management within the department through a structural process of objective setting, performance appraisal and individual development as appropriate.
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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.
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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 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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Create the clinical development strategy for one or more assets in collaboration with the global project team and internal partners such as clinical operations, translational medicine, regulatory affairs, biostatistics, drug discovery, drug safety, marketing.
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Leads strategic consultation, and guidance to the PV scientists on decisions that have significant drug safety implications, including safety signal detection activities of monitoring, evaluation, interpretation and appropriate management and communication of safety information for Insmed’s portfolio of products in development.
$339,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Demonstrated knowledge of principles of drug development, pharmacology, clinical trial methodology and design, medical monitoring of trials, assessment of drug risks and benefits, and safety assessment of drugs both on the market and in development and global safety regulations highly preferred.
$322,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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At least 5 years of experience as statistician supporting drug development and/or post marketing in Clinical research, Pharmaceutical company, CRO or Medical Device setting preferred. At least 5 years of experience as statistician supporting drug development and/or post marketing in Clinical research, Pharmaceutical company, CRO or Medical Device setting preferred.
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drug development jobs Title: director in Middlesex, NJ
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