55 Medical Writer jobs in United States available for remote work from home. Apply for positions such as Medical Writer, Medical Writer, Medical Writer and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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Develop and deliver scientifically accurate content across various projects while maintaining consistent style and quality. Collaborate with internal teams, clients, and key opinion leaders to align scientific content with account strategies.
The Medical Writer is responsible for designing, developing, and editing high-quality scientific materials such as slide decks, manuscripts, and meeting content. They also manage project timelines, collaborate with internal teams and clients, and mentor junior staff members.
The Medical Writer is responsible for drafting, editing, and coordinating scientific publications including manuscripts, abstracts, and posters. They collaborate with cross-functional teams to ensure all scientific content is accurate, compliant with ethical guidelines, and aligned with strategic objectives.
Collaborate with a multi-functional team to develop innovative medical and scientific educational materials for healthcare professionals. Consult with subject matter experts to create engaging content while ensuring accuracy through rigorous research and editing.
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The Medical Writer serves as the content lead for assigned accounts, developing scientifically rigorous and strategically aligned medical content. Responsibilities include conducting research, annotating content per AMA rules, and engaging with clients to provide subject matter expertise.
The Medical Writer creates high-quality scientific and clinical content for healthcare providers across various digital and live formats. They collaborate with medical experts and internal teams to ensure content aligns with program goals and industry regulations.
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.
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 Senior Medical Writer is responsible for creating high-quality, strategically aligned scientific content while leveraging AI-enabled tools to improve efficiency. They will manage client relationships, ensure scientific accuracy, and contribute to business development by identifying growth opportunities.
The Medical Writer II is responsible for preparing and leading the medical writing team on Phase I-IV study documents, including protocols, clinical trial reports, and investigator brochures. They must ensure all documentation meets regulatory, scientific, and ethical standards while coordinating review cycles with sponsors.
The Senior Medical Writer will lead the development of high-quality scientific materials and interpret clinical research data for diverse audiences. They will also provide editorial feedback to team members and participate in client and scientific meetings.
The Senior Strategic Medical Writer leads the preparation of clinical and regulatory documents to support drug and device development. They coordinate review processes, ensure compliance with international regulations, and collaborate with cross-functional teams to meet project timelines.
The Principal Medical Writer independently plans and prepares regulatory documents and medical communications to support product development. They are responsible for organizing, analyzing, and presenting scientific and statistical information in compliance with ICH and regulatory guidelines.
The Associate Medical Writer supports the scientific services team by developing technical content such as slide decks, manuscripts, and digital materials. They also manage project timelines, perform data checking, and actively research therapy areas to ensure high-quality scientific output.
The Senior Staff Medical Writer develops scientific and clinical documentation to support global regulatory compliance and market access for medical devices. They collaborate with cross-functional teams to synthesize clinical evidence and manage regulatory documentation throughout the product lifecycle.
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The QC Medical Writer is responsible for performing quality control audits of medical writing deliverables and ensuring adherence to company standards. They also support the team by facilitating document reviews and preparing clinical study documents such as protocols and reports.
The Principal Medical Writer independently plans and prepares regulatory documents and medical communications to support product development. They are responsible for analyzing, interpreting, and presenting scientific and statistical information in compliance with ICH and regulatory standards.
The Senior Medical Writer will lead document authorship for various clinical projects and serve as a project lead for smaller engagements. They will collaborate with delivery teams to produce high-quality regulatory documents while maintaining strong client relationships.
The Senior Medical Writer will lead the development of high-quality scientific written materials based on preclinical and clinical research data. They will also collaborate with team members, participate in client meetings, and ensure all deliverables meet project briefs and scientific standards.
The Principal Medical Writer leads the development of clinical documents and represents medical writing on multi-disciplinary teams. They are responsible for overseeing contract writers, ensuring regulatory compliance, and facilitating the review process for clinical documentation.
You will lead the development and execution of medical writing strategies for clinical research projects while ensuring high-quality deliverables comply with industry regulations. Additionally, you will collaborate with cross-functional teams and mentor junior writers to meet project timelines and publication objectives.
The Medical Writer will author and coordinate Clinical Evaluation Plans and Reports to support the Dental Solutions business unit. They will also collaborate with cross-functional teams to ensure clinical data compliance with EU MDR and other global regulatory requirements.
The Senior Medical Writer will lead clinical regulatory writing projects and serve as a key contributor to document authorship across various service lines. They will interface directly with clients and support complex engagements as part of a global delivery team.
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The manager will oversee the generation and quality control of clinical and regulatory documentation to ensure compliance with global standards. They will also mentor team members on technical writing best practices and manage document preparation timelines across various clinical programs.
The Principal Medical Writer leads the development of complex clinical documents and manages medical writing activities across various studies. They also provide expert peer reviews, mentor junior staff, and ensure all deliverables meet regulatory and client standards.
The Senior Medical Writer is responsible for developing, writing, and editing high-quality Medical Affairs materials, including manuscripts, abstracts, and scientific presentations. They will partner with cross-functional teams to ensure scientific accuracy and compliance while managing publication plans and external stakeholder outreach.
The Senior Medical Writer is responsible for developing scientifically accurate and strategically aligned content while managing research and project timelines. They also act as a client-facing lead, building rapport and providing subject matter expertise during team engagements.
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