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The village is also home of the famous landmark known as the Lower Falls Wine Company and the well-known author Sarah Fuller, who taught Helen Keller. magnetic resonance imaging technologist, magnetic resonance imaging, MRI technologist, MRI tech, MRI equipment, magnetic resonance, MRI, allied, allied health.
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Author regulatory submission documentation, including SRDs, IDEs, and PMAs. Ensure that software and data products are developed and validated to standards required for FDregulated products and/or for data included as part of a drug or diagnostic regulatory submission (e.g. SRDs, IDEs, Pre-Submissions, PMA.
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Now, our Business Intelligence team is looking for a Salesforce Dashboard Author who will transform complex data into meaningful visualizations and reports that effectively communicate insights and trends to Boston University’s Development & Alumni Relations (DAR) leadership and its stakeholders.
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Support project team lead to author technical reports and analytical Chemistry, Manufacturing and Controls (CMC) sections in regulatory documents. Senior Scientist Analytical Chemist. PhD in Analytical Chemistry, Biochemistry with emphasis in mass spectrometry.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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The Communications Director will compile and author a weekly report as directed by the Commissioner. The Communications Director shall coordinate with senior staff at MassDEP including the Chief of Staff, Deputy Commissioners, Government Affairs, and General Counsel, to plan and direct the Agency’s press strategy, including responding to media inquiries, sending press releases, coordinating social media, and managing press events.
$161,458.44 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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PK, dosimetry (radiopharmaceuticals), PK/PD and M&S component of study protocols, reports, project summaries and development plans, and author pharmacokinetic/clinical pharmacology/biopharmaceutics sections/radiation dosimetry of IND/IMPDs and NDA/BLAs as well as prepare appropriate responses to Health Authority questions across the globe.
$205,200 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Required Skills The successful applicant is expected to lead analyses and produce lead author publications based on the results, under the mentorship of experienced faculty. Required Experience The successful applicant is expected to lead analyses and produce lead author publications based on the results, under the mentorship of experienced faculty.
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Author and review SOPs, technical reports, and assist in the preparation of CMC regulatory submissions. Experience with qPCR, DNA and RNA extraction, ELISA, western blotting, UV spectrophotometry, DLS, MALS, mass spectrometry, and compendial testing will be a plus.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Experience with Apttus Shopping Cart functionality, Quoting, Word X-Author Templates. Experience with Apttus Advanced Workflow Approvals, Apttus Wizard, and X-Author for Excel Experience with Apttus admin settings, Apttus custom settings and EchoSign settings.
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Experience in peptide method development, characterization, and analytical control strategy, especially having mass spectroscopy (MS) experience. Provide analytical data to support drug substance and drug product development, including purity analysis, chiral purity and structure elucidation using mass spectrometry.
$143,832 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Job Title: GxP Data and CSV Engineer for mAlert Program Location: Remote Contract Type: Time and Materials Duration: 6 months with the potential for up to two years of support Job Overview: We are seeking a highly skilled and detail-oriented CSV Document Author & Integration Specialist to join our team on a contract basis.
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First author/lead author publications at leading AI and NLP conferences (such as EMNLP, ACL, ICLR, ICML, NeuRIPS) Proficiency with deep learning packages (such as PyTorch, Jax, or TensorFlow.
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Author journalism that offers readers both the analysis and careful explanatory take that is a hallmark of Globe reporting. The BGMP office is located in downtown Boston, near Faneuil Hall and Quincy Market, and is easily accessible by MBTA and commuter rail lines.
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Lead and author key pharmacovigilance documents, including medical safety assessments and regulatory responses, applying regulatory guidance for safety surveillance and document authorship. Minimum 10 years’ experience in drug safety/pharmacovigilance within clinical development.
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The candidate would be expected to draft and co-author papers, create presentation/ dissemination materials, and prepare PowerPoint slides and possibly IRB protocols. Experience with statistical programming using at least one of the following, a plus: STATA, SAS, Python, R.
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author job in Quincy, MA
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