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With a combination-focused pipeline that exploits the power of six scientific platforms (Immuno-Oncology, Tumor Drivers and Resistance, DNA Damage Response, Antibody-drug Conjugates, Cell Therapy, and Epigenetics) to help address unmet clinical needs in a host of cancers, we are motivated by a dedication to the scientific discovery and collaboration that will one day help eliminate cancer as a cause of death.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Masters degree in Pharmaceutical Science or related scientific field and minimum 8 years experience in pharmaceutical formulation and product development. PhD in Pharmaceutical Science or related scientific field and minimum 3 years experience in pharmaceutical formulation and product development.
ExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Excellent opportunity for an experienced Method Development Staff Scientist to join our rapidly growing team in Chantilly, VA. Labcorp Drug Development's work in developing new pharmaceutical solutions has an incredible impact on the lives of millions worldwide.
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Manage projects from initiation through closure for full scope regional and global projects, with activities focused on site selection, study start-up (including all systems and plan development), clinical operations, statistics and statistical programming, data management, subject randomization and drug supply management (IWRS), administration of data monitoring and/or adjudication committees, regulatory submissions, vendor management, and medical/scientific writing.
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Better predictive models for use in drug discovery and development will reduce the total number of animals used in the preclinical safety and toxicology assessment phase of the development of biologics, including reducing the use of higher species, in addition to supporting earlier attrition and reduced safety complication in the clinic.
$95,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Participate in senior level scientific, strategic, and operational aspects of drug development within the pharmacology, toxicology, and early stage clinical drug development process.
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The successful candidate will contribute to drug discovery efforts through analysis of multiple disease-relevant data sets, as well as development of core informatics pipelines and data organization.
$43 - $46 an hourExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Solid understanding of scientific principles and regulatory requirements relevant to global drug and drug-device combination product development, registration and post-market support.
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Understands the life sciences industry (e.g., CROs, pharma/biotech, medical device), scientific & clinical data/terminology, and the drug development process. MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.
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Interact and lead discussions with external authors and collaborators within the Medical Affairs, Drug Development, and Drug Discovery organizations to develop publication content related to Incyte studies.
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Youll provide expert anatomic pathology support to drug projects across all development stages. The role is broad in scope and offers significant potential for scientific collaboration and professional development.
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The Biotransformation group within the multidisciplinary DMPK organization at Eli Lilly and Company is seeking a scientific director to lead and implement biotransformation studies in drug discovery and development.
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Actively contribute to the development of regulatory strategies for investigational products in Investigational New Drug (IND)/ Clinical Trial Applications (CTA), Biologics Licensing Application (BLAs)/ Marketing Authorization Application (MAA), through evaluating scientific merits of Chemistry, Manufacturing and Control (CMC) and nonclinical study data package.
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Demonstrated experience with pharmaceutical drug development and the use of data analysis for strategy development, business process improvement, product launch planning, and integrated evidence generation required.
$183,000 - $280,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Areas of expertise include genomics, epigenetics, drug resistance, stem cell biology, drug discovery, diagnostics and biomarker development, and pharmacology. Minimum publication or in preparation of two articles as first author in high quality peer-reviewed scientific journals.
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