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You will oversee the flow of work across a variety of cookbook titles from editorial inception to finished books, centralize information, set milestones, help manage resources, and maintain schedules.
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Reporting to the Editorial Director, the Senior Editor will build a strong list of books in the social sciences of interest to both scholars and the general readership. Harvard University Press seeks a Senior Acquisitions Editor to sign 15-20 new books each year in psychology, sociology, and anthropology, as well as adjacent fields.
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Author and review Precision Medicine related sections in clinical study / regulatory documents (i.e. INDs, IBs, trial protocols/ops manuals, ICFs, IRB responses, HA Briefing Books, CSRs, etc) We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.
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Experience working with nonprofit organizations in the international development space including multi-country books consolidation preferred. Embrace technology like Google Workspace, Dropbox, Expensify, Slack, Keeper, Zoom, Gusto, and have experience integrating software with Quickbooks Online.
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You have the ability to maintain FDOT log books training will be provided. We are experts in cell tower construction, RF engineering, broadband fiber optic cable installation, OSP engineering, wireline construction, and emergency maintenance services.
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Act as the company liaison on CMC Regulatory matters and support related meetings, including preparation of briefing books, training, and preparing the technical team. The Associate Director, Regulatory Chemistry Manufacturing and Control (CMC) is accountable for executing global CMC regulatory strategies for our programs in early and late-stage development through and beyond approval.
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Screen Rant is the #1 entertainment website on the web and publishes up-to-the-minute news on blockbuster movies, TV, video games, and comic books. Note that this role does not involve video production, video editing, screenwriting, or writing reviews.
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Provides accurate, appropriate and timely drug information utilizing knowledge of pharmacology, reference books and scientific literature. Comprised of Tufts Medical Center, Lowell General Hospital, MelroseWakefield Hospital, Lawrence Memorial Hospital of Medford, Care at Home - an expansive home care network, and large integrated physician network.
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Contribute to regulatory communication and preparation of clinical sections of study and program level documents (e.g., protocols, ICFs, IB, briefing books, BTD, PIPs, SAPs, safety periodic reports.
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Is accountable for oversight of timely preparation and quality of Preclinical DMPK sections of regulatory documents (IND, NDA, briefing books, Investigator Brochures, etc.) The Global Drug Metabolism, Pharmacokinetics and Modeling (DMPK&M) department at Takeda is seeking a strong scientific and strategic leader to oversee a team of DMPK project representatives for supporting delivery of Takeda’s research and evelopment pipeline across GI, Neuroscience, and Oncology.
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Join us as a Scientific Director, Global DMPK&M in our Cambridge, MA location. This will include knowledge and experience of DMPK requirements for diverse modalities (e.g., small molecules, biotherapeutics) and potentially novel therapeutics (oligos, cell therapy.
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Completes medication station inspections are completed by designated Pharmacy Assistants (or in the absence of a Pharmacy Assistant by the Pharmacist). Participates in multidisciplinary team meetings, review discharge medication lists from skilled nursing facilities and inpatient hospitalizations, improve medication reconciliation process, and provide medication optimization consults for patients.
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Knowledge of Commercial and Government books of business – Medicare, Managed Medicaid, Fee for Service Medicaid. Reporting to the Sr. Director, US Value, Access, and Pricing, the Associate Director, US Payer Marketing will work closely with Market Access Colleagues (Payer, Patient Services), as well as US Marketing, Medical Affairs, HEOR, and Global Strategy to ensure alignment.
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With its proprietary FORCE™ platform, Dyne is developing modern oligonucleotide therapeutics that are designed to overcome limitations in delivery to muscle tissue. Lead CMC regulatory execution for specific programs at all stages of development.
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Develops and contributes to content, format and accountability for regulatory submissions and related supplements and amendments, including FDA meeting requests, briefing books, INDs, CTAs, orphan drug designations, pediatric plans, PRIME, BTD applications, DSURs, MAA/BLA/NDA, etc.
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books job in South Boston, MA
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