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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.
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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.
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In addition to work on IP specific activities the IPL will participate in standing committees, review post market surveillance trends, perform due diligence reviews, and consult to new business development on emerging market opportunities as well as contribute to the target product profile for new product development.
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Seeks professional development by monitoring one’s performance, solicits for constructive feedback, and leverages healthcare supervisor and store manager as mentor and coach. + Performs pharmacist tasks including compounding, drug therapy reviews, verification, and medication management.
$124,384 - $171,142 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Assists in interdisciplinary classification of inmates by identifying behavioral, emotional, organic, drug/alcohol, or personality problems and the subsequent development of appropriate programs on an individual basis.
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Direct experience in courseware development and delivery, including eLearning/CBT applications and design principles required. transforming ocular drug delivery. Support GxP and general business training processes, including training development and delivery.
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Previous work experience in presenting to, collaborating, or working from within global Public Health Agencies (World Health Organization, US Public Health Service Commissioned Corps, US Center for Disease Control - CDC, European Centre for Disease Prevention and Control -ECDC, US Food & Drug Administration – FDA, or equivalent), and/or Country, Regional, State, or Local Public Health Departments is preferred.
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5+ years in a leadership role related to scientific discipline, drug discovery or drug development desirable. Familiarity with compliance aspects of drug discovery and development (animal and/or human subject) is desirable.
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Proven track record of scientific leadership and accomplishments in biotechnology, with significant experience in drug discovery and development. Reporting to the CEO, the Chief Scientific Officer (CSO) will play a pivotal role in leading our scientific research and development efforts to drive scientific strategy and to shape the pipeline of novel CNS therapies.
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Depending on position, drug screen results and/or driving records, including minor moving violations, will be evaluated according to Coke Northeasts guidelines to determine eligibility for the position.
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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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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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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.
$29 - $30 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The ABC site, based in Worcester, MA, offers the unique setting where Biologics drug discovery, development and manufacturing coexist in one location. Take an active role in ML/AI roadmap development for novel antibody designs, driving information system infrastructure readiness for binding and functional assay data, and establishment of best practices in advanced knowledge base analytics.
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Minimum of 7 years experience in Good Manufacturing Practices (GMP) for biological drug development, with significant Chemistry, Manufacturing, and Controls (CMC) and ICH module 3 experience with experience in cell therapy and gene therapy CMC preferred.
$120,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago
drug development jobs in Westborough, MA
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