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Other clinical duties may include facilitating in-home diagnostics, point-of-care testing, administration of medications and other treatments, remote patient monitoring, clinical documentation, drain management, wound management, interpretation of diagnostic imaging & laboratory data.
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Strong laboratory skills and a high degree of attention to detail with the experience in following molecular biology and analytical techniques: PCR, gel electrophoresis, gel imaging, SDS-PAGE Mammalian cell culture, transfection, transduction (AAV) Nucleic acid preparation (DNA, RNA), ddPCR, qPCR and data analysis.
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Use sound scientific understanding of chemistry and chemical engineering fundamentals and an understanding of applied kinetics, thermodynamics, and transport fundamentals, as well as familiarity with modern laboratory instrumentation, automation, and laboratory/plant implementation of process analytical technology to contribute to the team's goals.
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The Kwon Laboratory ( at the Ragon Institute of MGH, MIT and Harvard at the Massachusetts General Hospital in Boston has an opening for a highly motivated postdoctoral fellow to study host-microbe interactions in the female reproductive tract that impact human health.
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Prior management of contract research organizations (CROs) for clinical biomarker assay development and qualification. Prior experience implementing precision medicine approaches in clinical trials including companion diagnostic (CDx) development experience in liquid-based and tumor tissue-based approaches.
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UMass Boston invites applications for a clinical assistant professor who will hold a full-time 9-month non-tenure track faculty position in the Department of Nursing. Collaborates with relevant administrative and support faculty for assistance and coordination with development of remediation plans when students are not meeting course or clinical objectives.
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At least 10 years relevant clinical drug safety/pharmacovigilance experience within the pharmaceutical or biotech industry, including 3+ years vendor oversight experience, required. You will be responsible for working with clinical, cross-functional study teams, and third party vendors/CROs to manage and support drug safety and pharmacovigilance operational activities and deliverables across Tango's clinical development portfolio.
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O working with analytical laboratories analysing research and clinical samples as part of laboratory routine work. The Director, Bioanalytical Diagnostic Development, will be responsible for defining the global bioanalytical development strategy and leading all activities related to clinical bioassays/diagnostics, from preparations for ‘first in human’ up to registrational studies and post-approval commitments.
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Experience working in a medical or clinical research setting (, psychology) EXPERIENCE: New graduates with some relevant course/project work or those without any prior research experience will be considered for the Clinical Research Coordinator I position outlined above.
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We are a full service consulting firm that provides consultants with the following expertise: Cerner, Epic, MEDITECH, Allscripts, eClinicalWorks, Athena, PeopleSoft, Lawson, SAP, Workday, Kronos, Premier, Population Health Management/Analytics, Legacy Application Support, Project Management, Business Analysis, Application Integration Analyst, Clinical Education, Top Flight University Talent, Revenue Cycle, HIM, Pharma, Life Sciences,BioInformatics, Clinical Engineering.
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The Associate Director, Clinical Data Analyst, has a critical role in the delivery of high-quality external data across Dyne's development pipeline by proactively identifying, measuring, and mitigating risk prior to acquisition of non-electronic data capture (EDC) data.
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The successful candidate will provide clinical data management oversight of outsourced clinical trials including but not limited to project management, vendor management, coordination of internal reviews, and approval of deliverables.
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PhaseForward Inform, Oracle Clinical and/or other clinical data management software desirable;General software skills: MS Access, MS Word, MS Excel, MS Project, Visio, familiarity with medical coding dictionaries, especially MedDRA and WHODRUG.Experience applying best practices in clinical data management programming in the clinical trial environment, including requirements definition and QC plansKnowledge of GCP and other regulations.
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Perform evaluation and selection of adequate technologies for establishment of clinical biomarker assays that meet clinical laboratory standards and regulatory requirements. Familiarity with clinical documents and processes, i.e. clinical protocols, informed consent forms, laboratory manuals, central lab logistics, etc.
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Generalist Med tech- coag, hem, ua, CHEMISTRY ETC. Job Duties/Responsibilities:Responsibilities are interchangeable within job titles of medical laboratory scientist (MLS), medical technologist or clinical laboratory scientist.
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clinical laboratory jobs Title: project director in Boston, MA
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