Medical Writer Jobs - Remote Work From Home & Flexible
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24 days agoWriteand review synopsis and Clinical Study Reports/Clinical Investigation Reports. Prepare protocols, monographs, patient narratives, and manuscripts for journal publications. Review of Statistical Analysis Plans.WriteClinical Study Protocols...
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New!3 days agoConduct proofreading, editing, document formatting, review comment integration, and document completion/approval activities. Previous PSURwritingexperience or experiencewritingdocuments relevant to EU MDR. Knowledge of EU MDR. University degree...
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New!3 days agoThe PrincipalMedical Writeris responsible for providing clinical regulatory document support and advancedmedical writingexpertise to the clinical teams, ensuring successful preparation of high-quality submission-ready documents and effective...
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18 days agoAct as a leadmedical writeron several projects from simple to complex level. Produce clinical documents as required. Provide scientific andmedical writingconsultancy to clients and internal colleagues at a moderate level. Lead project teams...
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24 days agoAct as a leadmedical writeron several projects from simple to complex level. Produce clinical documents as required. Provide scientific andmedical writingconsultancy to clients and internal colleagues at a moderate level. Lead project teams in...
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New!4天前TheMedical Writer(MW) will providewritingassistance on various documents, including safety narratives, clinical study reports (CSRs), Development Safety Update Reports (DSURs), and other documents, as needed. This position will be responsible for...
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30+ days agoManage execution of documents, including creating, maintaining, and communicating timelines. Coordinate cross-functional client contributors and stakeholders as well as internal resources (e.g., quality control [QC], publishing). Serve as an expert.
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30+ days agoCarry outmedical writingactivities in accordance with client specifications in a timely, accurate, and efficient manner, and to the written, scientific, and ethical standards in accordance with regulatory requirements and WCT standard operating...
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8 days agoCarry outmedical writingactivities in accordance with client specifications in a timely, accurate, and efficient manner, and to the written, scientific, and ethical standards in accordance with regulatory requirements and WCT standard operating...
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New!3 days agoAssists in activities related to the preparation and compilation of data and information into a single comprehensive package for new and updated regulatory documents (US and ex-US). Serves asmedical writingsupport to otherwriters. Learning US...
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30+ days agoWriteIND modules, NDA modules & other related regulatory documents.Writeclinical study reports, protocols, and protocol amendments. Coordinate quality control reviews of documents and maintain audit trails of changes. Interact closely with sponsor.
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Featured18 days agoReviews routine documents prepared by junior team members. May provide training and mentorship for juniorwritersand program managers on document preparation, the use of software for document development, document types, regulatory requirements, and...
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FeaturedNew!6 days agoLeverages experience as amedical writerto serve as a subject matter expert formedical writingdeliverables. Works with a diverse client base with exposure to a variety of therapeutic areas, indications, and therapeutic innovations.
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15天前Provide leadership to the Clinical and RegulatoryMedical Writingteam and the broader Scientific Information and Publications (SIP) department as a member of the SIP Leadership Team. Recruit, train, and supervise internal staff and contractwriters.
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New!3 days agoServes asmedical writinglead on more complex clinical regulatory documents, such as those associated with dossiers for regulatory filings and CERs compliant with MDR. Implements all activities related to the preparation and compilation of data...
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30+ days agoYou will have the ability to utilize yourmedicalexpertise and perfect your research andwritingcraft while working from home and creating your schedule. Producing clean, in-depth content in a timely fashion for law firms andmedicalpractices across...
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13 days agoWorks effectively with cross-functional groups to produce high-quality, scientifically accurate documents under strict timelines, and ensures consistency between related documents. Responsible for ensuring that assigned documents undergo a quality...
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30+ days agoProvide in-depth knowledge of analysis and presentation of scientific and/or clinical data in regulatory documents. Work independently on routine documents, with the primary deliverables of this role being clinical regulatory documents consistent...
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30+ days agoLead the content planning and production of written research findings (abstracts, manuscripts, systematic reviews, presentations, etc.) or regulatory documents (protocols, investigator brochures, clinical study reports, etc.) that aligns with...
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30+ days agoIn this position, you will have the ability to utilize yourmedicalexpertise and perfect your research andwritingcraft while working from home and creating your schedule. Producing clean, in-depth content in a timely fashion for law firms and...
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26 days agoThe PrincipalMedical Writeris responsible for development and management ofmedical writingdeliverables that support the clinical regulatorywritingportfolio and is capable of working independently to achieve goals. Applies in-depth knowledge...
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30+ days agoWork with regulatory and clinical teams towriteand/or review clinical and regulatory documents and oversee all reportwritingactivities to support BLA filing. Provide appropriate background information, guidance, and training to colleagues...
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30+ days agoIn this high visibility role, the individual will be responsible for independentlywritingand managing clinical study-related documents including, but not limited to, clinical study protocols, Investigator's brochures, and clinical study reports.
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30+ days agoScientific Director is responsible for leading and developing materials/content for account-associated activities (including scientific direction and strategy, project management), as well as applying expert knowledge of the market, therapeutic area...
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30+ days agoProviding research andwritingsupport to assigned brand teams and new business efforts. Working independently and as part of a multidisciplinary team that includes amedicaldirector, editor, graphic designers, and account personnel. Producing...
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30+ days agoOur SeniorMedical Writerswork as part of a multidisciplinary team (includingmedicaldirector, editor, graphic designers, and account personnel) to produce abstracts, posters, outlines, primary and review articles, monographs, slide presentations...
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30+ days agoPrepares and delivers effective presentations for internal and external audiences, as needed. Participates in discussions regardingMedical Writingprocess strategy. Master's Degree and 4+ years of relevant work experience, or Bachelor's Degree and 6+...
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30+ days agoAuthors routine clinical and regulatory documents (e.g., clinical study protocols, clinical study reports, and investigator's brochures, and sections of regulatory submissions) in partnership with cross-functional team with oversight. Supports clinical...
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30+ days agoUnder minimal supervision, theMedical Writerwill critically evaluate, analyze, and interpret themedicalliterature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias.
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30+ days agoThe ProposalWriterConsultant supports live bids and future bids bywritingand editing proposal sections, individual answers, and new library content. The consultant will complete content tasks identified by RFP Lead, Sales, and Proposal Managers to...
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23 days agoAlongside a growing team of editors andwriters, you'll concept andwriteeducational financial content, including video and audio scripts, articles, news bulletins, financial literacy courses, and short-form and in-app copy. We're looking for someone...
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New!3 days agoTheMedicalCommunications Manager ofMedicalAffairs will be responsible formedicalcontent development,medicalreview and approval,medical writing, literature surveillance and competitive intelligence, and Veeva MedComms Management. Remote.
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30+ days agoSourcing, curating, and aggregating interesting, important information for a daily newsletter.Writingquickly, accurately, and well, with a consistent eye to audience needs, grammar, style, and accessibility. Crafting compelling, conversational...
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9 days agoThe main function of a ContentWriteris towritetechnical materials, such as equipment materials, appendices, or operating and maintenance instructions. A typical technicalwriteris responsible for organizing, editing and maintaining technical records.
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25 days agoAnalyzing, developing proposal compliance matrices,writing, preparation, and submitting RFI and Sources Sought requirements Developing win themes and strategies. Developing proposal outlines, compliance matrices, andwritingproposal content.
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30+ days agoCreate stories with interesting characters and compelling narratives, follow the established style and tone of our games,writefrom a variety of perspectives, accept and incorporate feedback, adaptwritingto meet requirements, and meet deadlines.
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30+ days agoAs a TechnicalWriter, you'll be supporting our commercial and construction customers through engaging and effective documentation, including release notes, training content, and supporting documentation for new features, product improvements, and...
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23 days agoAlongside a growing team of editors andwriters, you'll concept andwriteeducational financial content, including video and audio scripts, articles, news bulletins, financial literacy courses, and short-form and in-app copy. We're looking for someone...
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30+ days agoThis individual will be responsible for leading projects, red lining documents, as well as creating documents. The ideal candidate should have experience following site instructions towriteSOPs from scratch as well as strong project management skills.
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30+ days agoProvide technicalwritingand editing support, including preparation of programmatic and engineering documentation for the client. Experience with military standards and specifications governing the preparation of technical documentation.
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30+ days agoResearch, create and deliver high-quality content to biotech/pharma clients according to specified deadlines. Ability towriteto a high-level audience (specifically scientists). Comfortable with scientific jargon and vocabulary. Edit the work of peers...
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12 days agoSeeking an experienced ProposalWriterwith experience developing technical proposal content, researching technical areas, and interviewing subject matter experts towritecompliant and compelling proposal sections, including technical, management...
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30+ days agoThe TechnicalWriterworks with the project team to structure and review draft reports. Serve as point of contact for report reviews, consolidation of comments/proposed changes, and comment adjudication. Assist in the finalization of plans, analyses,...
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22 days agoAssist inwritingand/or editing technical documents, including business proposals, reports, user manuals, briefings and presentations, functional descriptions, system specifications, guidelines, special reports, and other project deliverables to meet...
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24 days agoAuthor easy-to-understand customer-facing guides and Help articles that meet style and editorial standards. 1 year experience in technicalwritingor other non-fiction, technical, or educational content. Manage tasks and needs for assigned areas from...
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Featured1 week agoResponsible for development of responses for moderately complex proposals questionnaires and surveys through project management, research, data gathering, analysis,writingand editing in accordance with brand standards, plain language and internal RFP...
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22 days agoFreelance, remote role. Requires MA and STEM experience, plus professionalwritingskills. Create technical documentation and meet project requirements, and ensure client specifications are met.
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12 days agoProvide TechnicalWritingand copy editing support across content to support the business. Ability to edit technical and non-technical content written by others, catching duplicative copy, repeat messages, standard copy-editor responsibilities, and...
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2 weeks agoWritten and visual communication of complexmedicaldevice equipment into clear and concise outputs for internal and external use. Work with Subject Matter Experts and study drawings, specifications, mock-ups, and product samples to develop content.
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15天前Plan, coordinate, andwrite拨款提案,包括所有必需的支持materials, in collaboration with relevant staff members and approval of Chief Partnerships Officer. Craft grant proposals that are well-researched and customized to adhere...
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