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The Clinical Trial Associate, SSU will aid in study start up activities for Fractyl's global clinical program, draft SSU documents, site regulatory document review and approval, and IRB/EC and regulatory submissions and approvals.
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The study also encompasses an examination of plant cell anatomy and the chemical content of xylem sap. Post Doctoral Fellow – Plant Biotechnology and Ecophysiology Posted: February 5, 2024 Position Code: 1109 Position Overview Merrimack College is looking for a highly motivated postdoctoral candidate with plant molecular biology and biotechnology background to work on a newly funded project to investigate the mechanism of silver nanoparticles translocation in L. esculentum.
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Job DetailsDescription Position Title: HS/PRS Regional Supervisor/Lead Case ManagerReporting Relationship: Assistant Program Director HS/PRS Position Summary NYAP’s Home Study/ Post Release Services (HS/PRS) Regional Supervisor/ Lead Case Manager (RS/LCM) is responsible for providing direct supervision and oversight of the Home Study and Post Release Services (HS/PRS) process of an assigned region under a grant from the Office of Refugee Resettlement (ORR.
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Position OverviewMerrimack College is looking for a highly motivated postdoctoral candidate with plant molecular biology and biotechnology background to work on a newly funded project to investigate the mechanism of silver nanoparticles translocation in L. esculentum.
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Experience with engineering calculations such as:load flow, short circuit and reactive capability analysis (ETAP or SKM), Arc flash analysis (ETAP or SKM), Cable ampacity study (CYMCAP or equivalent), grounding analysis, AC-DC voltage drop calculations, VOC/ISC calcs, AC/DC Cable sizing.
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Study nanoparticle-membrane interaction mechanisms using analytical methods like fluorescence spectrophotometry, inductively coupled plasma mass spectrometry (ICP-MS) and Gel permeation chromatography (GPC.
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Complete all CTN required trainings, such as Human Subjects Protection and Good Clinical Practice, as well as study specific training (e.g., assessments, data entering and management procedures, and using the data management system), and MGH IRB and Research Management required trainingb.
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Interfaces with physicians and scientists for study conduct and regulatory compliance for investigator sponsored trials in a global environment. Ensures IST study files meet GCP requirements, regulatory requirements (including drug accountability) and accurately reflect the content and status of all IST's.
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Polysomnography records your brain waves, the oxygen level in your blood, heart rate and breathing, as well as eye and leg movements during the study. Polysomnography records your brain waves, the oxygen level in your blood, heart rate and breathing, as well as eye and leg movements during the study.
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Perform study start-up and conduct activities including ICF review that meets regulatory requirements, creating study specific essential document lists, managing and communicating the status of study progress and activities.
$95,000 - $125,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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This role will collaborate closely with key cross-functional internal stakeholders including Clinical Operations, Medical Monitoring, Data Management, Supply Chain, and Clinical Compliance and Quality as well as external CRO and vendor partners to ensure quality study oversight from study start up through close out.
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Interact with the bioanalytical, in vivo teams and customers on scientific study designs, protocols, adverse events, shipping details, and reports. This includes timely and accurate communication with customers on protocols, adverse events reporting, and study timelines.
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Degree (or higher) in Environmental Science, Biology, Ecology, Wildlife Biology, Natural Resource Management, or a related course of study. degree (or higher) in Environmental Science, Biology, Ecology, Wildlife Biology, Natural Resource Management, or a related course of study.
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Author and execute study protocols governing bioanalytical studies to support in vivo studies and sample analysis. The Scientist will play a role in the design and qualification/ validation of study methodologies to support in vivo studies while supervising a team of up to 2 scientists.
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OR You may substitute education for specialized experience as follows: At least one (1) academic year of progressively higher-level graduate education leading to a graduate degree in a related field of study such as: human resources, public administration, organizational psychology, or other administrative and management fields.
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study job Company: Genoskin in North Reading, MA
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