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At the late shift you may at times be working without direct management oversight, so your responsibility is seen as even greater as you assist in closing out the business for the day as well as checking in or out guests during non-traditional hours.
$26.78 an hourFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Lead the analytical development activities for early and late late-stage clinical products at CMO/CRO. The Lead of Quality Control and Analytical Development is responsible for managing a team that provides quality oversight in support of clinical and commercial operations and analytical development of early and late-stage clinical products.
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Partner with a team of dedicated and senior Clinical Biomarker scientists on the science and bioanalytical assays for Moderna's early and late phase infectious disease vaccine programs. The Director will work collaboratively across multiple clinical teams to ensure strategy, planning, execution and data delivery of biomarker lab data for early and late phase infectious disease vaccine clinical trials conducted by Moderna.
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Join Takeda as a Scientist – Analytical Development (AD) – Late Stage Development where you will independently lead efforts in development of analytical methods, implementation of evolving scientific technology and influences strategic planning within AD and across Pharmaceutical Sciences to deliver on program strategy and initiatives.
$170,500 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Work collaboratively with the toxicology team and future translational pharmacology and clinical development teams to support the progression of therapies from late discovery through first in human clinical studies integrating DMPK data into the overall drug development strategy.
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Early and late-stage regulatory CMC program/project leadership (Phase I/II and Phase III IND/CTA, MAA/BLA) and experience with non-viral or viral vectors is desirable. Provide regulatory CMC strategic leadership to support the development of early and late-phase gene and cell therapy products for the treatment of genetic diseases.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Keywords : senior director, clinical program lead, late-stage clinical development, clinical trials, global, strategy, hematology, lymphoma, oncology, targeted therapies, ADCs, antibody-drug conjugates, program, asset, label extension, life-cycle management, pharma, biotech, biopharma, MD, medical doctor, phase I, phase II, phase III, FDA.
Full-timeRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Design and drive negotiations with regulatory agencies globally in preparation for late-phase clinical development and marketing applications. This opportunity will offer you the chance to grow your Regulatory Affairs CMC expertise across a range of disciplines such as nucleic acid therapeutics, lipid-nanoparticle drug delivery, viral delivery systems, and a range of cell therapy products.
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Reporting to the Senior Vice President, Technical Development, this role is critical to advancing novel drug delivery technology from Research to the clinic and on to late phase development and commercialization as a member of the Technical Development Leadership Team the role also plays a significant role across the function.
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The Analytical Development- Waltham team is responsible for late-phase to commercial method development, optimization, validation, advance characterization, process development support, regulatory authoring, and control strategy for ADCs. The team works cross-functionally with process development, regulatory, and quality with the Abbvie network and with contract manufacturing organization and contract laboratories.
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3+ years of medical safety leadership experience, inclusive of establishing program-level safety strategy, proactive signal detection & evaluation, risk identification & mitigation planning for early and/or late-stage clinical assets, preparation & authoring of periodic safety reports, Risk Management Plans, health authority responses, and supporting NDA/BLA/MAA submissions.
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This is a late stage Pharma/Biotech company focused on the development and pioneering of cell therapy candidate’s that aim to transform the treatment of Chronic Kidney Disease. Experience with global clinical trial operations, in multiple phases of research, including late stage.
$175,000 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Representing Biomarker Development on Cardiovascular and Metabolism early and late Disease Area Decision Boards to identify, develop, and drive cardiovascular and metabolic disease and compound mechanistic biology, and precision medicine approaches for the portfolio.
$249,600 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The successful candidate will have 10+ years of process development experience with direct experience in AAV and late-stage molecular biologics development, including participation in projects involving cross-functional teams.
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Medical Lab Scientist
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late shift jobs Title: room Company: Trusted Health in Roslindale, MA
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