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Abbvie is seeking a highly motivated and experienced translational scientist to lead a team of senior scientists accountable for driving the development, planning, and execution of the clinical translational research and precision medicine strategy across the rheumatology drug pipeline at Abbvie.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Astellas Institute for Regenerative Medicine (AIRM) is a wholly-owned subsidiary of Astellas Pharma Inc and focused on the development and commercialization of stem cell and regenerative medicine therapies.
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General understanding of biopharmaceutical development, clinical research, biologics manufacturing, cell therapy manufacturing. The Supply Chain Analyst I will provide input and oversight to ensure all operations meet, or exceed, cGMP regulations, guaranteeing high level of quality of the Drug Substance and Drug Product Processes.
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About Safety Assessment Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance.
$19 - $21 an hourFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
$25ExpandUpdated 10 days ago - UpvoteDownvoteShare Job
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This position will participate in, and may oversee, prospective and retrospective DUR activities including, but not limited to: handling live calls from physicians and pharmacists, reviewing appropriate drug therapy, coordinating and managing the request for prior authorization process, participating in the development of clinical drug use criteria, and the coordination of activities of the clinical workgroups of program advisory boards.
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Please be advised that due to the nature of this position, incumbents are subject to federal Drug & Alcohol safety regulations governing US Department of Transportation ("DOT") covered positions, including the Federal Motor Carrier Safety Administration (FMCSA) and Pipeline Hazardous Material Safety Administration (PHMSA.
$24.41 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Oversee case management services which may include drug testing coordination, treatment adherence monitoring, referrals to other services and levels of care (including detox, inpatient and residential care), health insurance application assistance, transportation, and communication with probation and the courts.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Job Description Primary responsibility is to advance multiple research projects from Lead Optimization through Candidate Selection stages through effective leadership of matrixed, multi-disciplinary teams with membership from discovery, precision medicine, preclinical safety and safety pharmacology, DMPK-BA, CMC, clinical development, and others.
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Clear understanding of the drug development process, submission-related activities and regulatory requirements (eg, CDISC, CDASH, eCTD) and guidelines (eg, ICH, CHMP, FDA, GCP). Provide input on programming methodologies to support the clinical development process.
RemoteExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance.
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Work with cultured cell lines and primary cells from multiple species (murine, human) using sterile technique to perform assay development, model characterization, and screening. As part of the Oncology Drug Discovery Unit (ODDU), you will report to Associate Director, reporting into the Tumor Biology Lab Head within the group.
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The Formulation Senior Research Associate will work with other scientists dedicated to clinical parenteral drug product development of an array of molecule modalities (protein, oligonucleotide, small molecule, etc.
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Thats why we offer competitive wages and a wide range of benefits, including medical and dental insurance, prescription drug card, 401K and pension plans, flexible dependent care and medical spending accounts, spouse and child life insurance, employee referral bonus, and discounts with Penske partners.
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Analytical Laboratory experience, specifically addressing upstream process development and/or large molecule characterization applications in pharmaceutic drug development to help customers accelerate their process.
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drug development jobs in Worcester, MA
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