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The Department of Psychiatry and the Behavioral Sciences at the Keck School of Medicine of USC seeks an experienced Senior Grant Writer to research, draft, and submit proposals to support clinical and translational mental health research activities.
$64,480 - $66,168 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Client is an on-demand, autonomous ride-hailing company hire a Technical Writer to author and maintain BaseOps technical documentation to support technicians/engineers with managing our autonomous vehicle fleet.
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We are looking for a Technical Writer with a Secret clearance or higher to join our Naval Surface Warfare Center Team! Technical Writer - Secret Clearance. Help author reports, plan and strategy documents, and meeting minutes.
$65,000 - $85,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Author and publish the documentation suite for each infrastructure project for two core audiences (online HTML knowledge articles for global Operations Support teams authored in ServicePoint Knowledge Management System, and infrastructure reference guides for Platform Engineering authored in MS Word.
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Data analytic publication experience or literature author publication experience. As an Associate Clinical Writer, you will work within the Clinical Affairs team. In addition to a competitive base salary, we also offer bonuses and other applicable incentive compensation plans that can further increase your total compensation package We want to invest in your growth and development, which is why we provide training opportunities with ongoing learning and development courses.
$65,000 - $75,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Labcorp are recruiting a Lead Medical Writer to work outsourced to one of our clients. - Search literature databases for relevant information, recommend label changes, author proposed label text and preparation of supporting/justification document.
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Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias.
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Substantial clinical study protocol experience, as lead author, required. MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.
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Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, presentation materials and publications to medical journals.
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MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, including clinical trial transparency,and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.
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Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards.
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Bachelor’s, Masters or PhD Degree in scientific, medical, clinical discipline or related field is required with at least 6 years of previous regulatory writing experience; Masters or Phd degree is preferred.
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Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.
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Not required, but experience with orphan drug designations and PSP/PIPs a plus. The ideal candidate would hold a Bachelors, Masters, or Ph. D. in scientific, medical, clinical discipline. Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools.
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4, and 2.5 documents, presentation materials and publications to medical journals. Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects.
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