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Reviews, analyzes, and summarizes data to be used in clinical study reports or other high-quality scientific communications and regulatory documents. The Director/Senior Director in Medical Writing will provide leadership, direction, and competence for the development of high-quality clinical research documentation that adheres to departmental standards and regulatory guidelines, in support of drug development, product registrations, and product marketing to meet the company’s global strategic, scientific, regulatory, and commercial goals.
$265,800 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Ensures quality in all deliverables and documentation with attention to detail, consistency and integrity of data. Effectively communicates and collaborates with Sales and Marketing, R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs, Clinical Science, Risk Management and Medical Affairs in completing clinical evaluation project related deliverables.
$45 - $50 an hourPart-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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The Senior Medical Writer is expected to develop and maintain a network of internal relationships with global and local cross-functional study teams, including personnel from Medical & Science, Clinical Pharmacology, Biostatistics, Clinical Operations, Regulatory Affairs, Global Safety, Data Management, and Non-clinical Development.
Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Quality/Compliance: Critically analyzes and evaluates the rendering, display, and presentation of scientific and therapeutic data for use by internal stakeholders to respond to Medical Information Requests (MIRs.
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Plan, develop and lead the completion of complex medical writing projects in a fast-paced environment with accountability for successful completion within scope of project deliverables including negotiating deliverable timelines, and resolving project-related issues with cross-functional partners (e.g., Regulatory Affairs, Quality, Clinical Project Managers, Clinical Data Management, Biostatistics, etc.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Experience as a medical writer for a medical device company, cardiovascular medical device company highly preferre. In understanding the challenges of open-heart surgery, we partner with surgical teams to deliver modern technologies intended to enhance patients’ quality of life and expand their potential treatment opportunities.
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In addition, the CER Writer/PM will interact cross-functionally with various personnel to identify and obtain relevant documentation and data on safety, performance, adverse events and risk/benefit profile of a device or devices.
$167,200 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Recent experience as a medical writer for a medical device company (class II or III) required; cardiovascular medical device company highly preferred. Extensive knowledge on conducting focused searches within medical literature databases (e.g., PubMed, Medline) and ability to evaluate/summarize content.
Full-timeRemoteExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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This includes conducting searches of peer-reviewed publications, risk management files and post market quality tabulations to compile relevant data. The Senior Medical Writer is primarily responsible for preparing Clinical Evaluation Reports (CERs) and associated documents for regulatory submissions and Post-market Surveillance for analysis of existing product clinical performance, while working in a cross-functional team.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Provide mentoring and knowledge transfer for Medical Writing team members. The Medical Writing Manager will provide guidance, develop, and lead medical writing projects , timelines and activities.
$59.82 an hourTemporaryRemoteExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Effectively communicates and collaborates with Sales and Marketing, R&D, Regulatory Affairs, Quality Engineering, and Medical Affairs in completing clinical evaluation project related deliverables.
$38 an hourExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Drawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Ensure quality in all deliverables and documentation with attention to detail, consistency, and integrity of data; responsible for compliance with applicable corporate and divisional policies and procedures.
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The Principal Medical Writer position is responsible for authoring medical writing deliverables with a focus on quality, accuracy, and efficiency, and provides medical writing support to ProPharma clients.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Interfaces with functional groups (e.g. PK, Toxicology, Regulatory, Statistical Support, Data Management, Clinical) and writers (internal and external vendors) to ensure timely completion of projects that are scientifically accurate and of high quality.
Full-timeRemoteExpandApply NowActive JobUpdated 28 days ago
data quality jobs Title: medical writer in LA, West Virginia
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