The Medical Writer is responsible for preparing and quality-checking clinical documents, including protocols, CSRs, and scientific publications. They also handle document e-publishing and may serve as a DMC Administrator to coordinate committee meetings and charters.
Remote Medical Writer Jobs (109)
Search = Medical Writer
Develop medical affairs and publications content across three different workstreams. Create high-quality materials that align with client strategic marketing goals and scientific credibility.
Lead the development of high-quality scientific written materials and innovative medical communications projects. Review and interpret preclinical and clinical research data to create content for physician and consumer audiences.
The medical writer manages and oversees the production of high-quality clinical documentation, including protocols, reports, and regulatory briefing materials. They ensure all documents meet scientific accuracy, regulatory guidelines, and established templates for submission to authorities.
The Medical Writer reviews medical records to draft narrative summaries for Medicare Set Asides and Medical Cost Projections. They ensure all documentation is accurate and consistent with client protocols and internal guidelines.
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The Medical Writer is responsible for developing high-quality clinical documentation, including site manuals and charters, while ensuring compliance with regulatory standards. They will review study protocols, eCRFs, and SOPs to maintain accuracy and consistency across clinical studies.
The role involves writing and updating Clinical Evaluation Reports (CERs), PMCF reports, and SSCPs to comply with international regulations. It also requires analyzing clinical data and collaborating with cross-functional partners to respond to regulatory agency requests.
Lead the planning, writing, and editing of high-quality regulatory documents including CSRs, IBs, and eCTD summaries for clinical drug development. Collaborate with cross-functional teams to analyze scientific data and respond to health authority requests.
The primary role involves developing accurate, high-quality, and compliant medical and scientific content based on clinical data, publications, and medical insights. This includes creating various materials like slide decks, manuscripts, and medical information pieces while ensuring scientific accuracy and adherence to standards.
The primary role involves developing accurate, high-quality, and compliant medical and scientific content based on clinical data, publications, and medical insights. This includes creating various materials like slide decks, manuscripts, and medical information pieces while ensuring scientific accuracy and adherence to standards.
The Medical Writer will perform internal Quality Control (QC) procedures for various clinical documents and act as a lead writer in preparing clinical documents or scientific publications, adhering to established timelines and styles. Responsibilities also include performing literature searches, document e-publishing, and potentially serving as a Data Monitoring Committee (DMC) Administrator or Secretary.
Leads the creation and accurate completion of medical writing deliverables, including clinical study reports, protocols, and manuscripts. Coordinates with cross-functional teams and clients to ensure documents meet regulatory standards and project budgets.
Senior Medical Writer
Everest Clinical Research
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Full Time
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23 hours ago
Everest Clinical Research
Author accurate regulatory documents such as CSRs, protocols, and IBs to support clinical trial authorizations and marketing applications. Lead writing projects from initiation to close-out while managing sponsor relationships and performing peer quality reviews.
The Senior Medical Writer leads the development of high-quality scientific materials and innovative medical communications projects. Responsibilities include interpreting clinical research data, conducting literature searches, and synthesizing trial data for physician and consumer audiences.
Lead the preparation and writing of clinical and regulatory documents for drug and device development. Coordinate reviews and quality control processes to ensure compliance and timely delivery of submission objectives.
Lead the preparation and writing of clinical and regulatory documents for drug and device development. Coordinate review processes and ensure high-quality, compliant submissions within project timelines.
Lead the development of high-quality regulatory and clinical documents to support submissions to regulatory authorities. Coordinate writing assignments, formulate strategies, and ensure compliance with industry standards and sponsor requirements.
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The Senior Medical Writer leads the authorship of clinical regulatory documents and manages smaller projects while supporting larger engagements. They interface directly with clients to ensure goals are met and maintain professional business relationships.
Lead the creation and accurate completion of medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinate with cross-functional teams and clients to ensure scientific clarity and adherence to regulatory standards.
Develop clear and accurate scientific content across various medical communication deliverables while ensuring strategic alignment and scientific integrity. Lead assigned projects, manage client expectations, and mentor junior medical writers.
The Principal Medical Writer plans and prepares regulatory documents and medical communications to support all phases of product development. They are responsible for analyzing and presenting scientific and statistical information in accordance with ICH and regulatory guidelines.
The role involves authoring various aggregate safety reports and serving as a project lead for smaller engagements. The writer will interface directly with clients and collaborate with larger delivery teams on complex projects.
Leads the creation and coordination of clinical and regulatory documents, ensuring scientific accuracy and adherence to regulatory standards. Acts as the primary technical contact for internal teams and clients while mentoring junior medical writers.
Senior Regulatory Medical Writer, Client-embedded, FSP
Thermo Fisher Scientific
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Full Time
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1 Week Ago
Thermo Fisher Scientific
The Senior Medical Writer authors routine and complex clinical regulatory documents, including study reports, protocols, and INDs. They collaborate with cross-functional teams to ensure document accuracy and mentor junior medical writers to maintain high-quality deliverables.
Lead the development of clinical study documents and regulatory submissions while collaborating with cross-functional teams to analyze trial data. Provide strategic input for clinical development programs and mentor junior medical writers to ensure high-quality scientific output.
Senior Medical Writer - Medical Information
Thermo Fisher Scientific
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Full Time
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1 Week Ago
Thermo Fisher Scientific
The Senior Medical Writer creates high-quality medical information documents, publications, and clinical study documents for internal and external clients. They are also responsible for reviewing team deliverables, mentoring new hires, and potentially assisting with program management activities.
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Medical Writer I (Junior Project Specialist - 1 year Contract)
Syneos Health
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Full Time
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1 Week Ago
Syneos Health
The role involves managing compliant document filing and eTMF activities within the Veeva RIM system. It also requires maintaining project timelines and collaborating with stakeholders to ensure regulatory standards are met.
The Principal Medical Writer will lead the development of high-quality scientific content across various therapeutic areas and ensure compliance with industry standards. Responsibilities include conducting literature reviews, managing writers, and preparing materials for promotional review processes.
Associate Director, Medical Writer
MannKind Corporation
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Full Time
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2 Weeks Ago
MannKind Corporation
Lead the preparation and production of high-quality, ICH-compliant regulatory and scientific documents including protocols, CSRs, and submission documents. Coordinate cross-functional teams to ensure alignment with corporate milestones and maintain global regulatory compliance.
Associate Director, Medical Writer
MannKind Corporation
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Full Time
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2 Weeks Ago
MannKind Corporation
Lead the preparation and production of high-quality, ICH-compliant regulatory and scientific documents including protocols, CSRs, and IB. Coordinate cross-functional reviews and provide strategic medical writing oversight for multiple compounds across various therapeutic areas.
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