140 Medical Writer jobs 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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The medical writer will research, write, and edit regulatory documents such as protocols, investigator brochures, and clinical study reports while coordinating with authors and stakeholders. They will also act as a project manager for writing deliverables, ensuring adherence to industry standards and timelines.
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.
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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.
The Medical Writer will author, edit, and finalize high-quality expert reports and statistical analysis plans for cardiac safety studies. They will collaborate with cross-functional teams to interpret clinical data and ensure all documentation aligns with regulatory expectations.
Develop high-quality scientific and clinical content for healthcare providers across various digital and in-person formats. Collaborate with medical experts and internal teams to ensure content aligns with program goals and industry regulations.
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 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.
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 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 I is responsible for the end-to-end preparation, quality control, and lifecycle management of clinical and regulatory documents. They also manage document workflows within the Electronic Document Management System and ensure compliance with GxP and ICH guidelines.
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.
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Develop high-quality scientific and medical materials such as manuscripts, abstracts, and posters while ensuring strategic alignment and scientific accuracy. Provide mentorship to junior writers and collaborate with international pharmaceutical clients to execute effective medical communications initiatives.
Lead the development and execution of medical writing strategies for clinical research projects, including the creation of clinical pharmacology and pharmacometrics documents. Ensure all deliverables are inspection-ready, compliant with regulatory requirements, and effectively communicated to project teams.
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 Medical Writer is responsible for planning, coordinating, and authoring high-quality clinical and scientific documents such as study reports and protocols. They also collaborate with internal and external teams to ensure operational excellence and compliance with regulatory requirements.
The role involves leading the preparation of complex regulatory medical writing deliverables while ensuring scientific accuracy and adherence to regulatory standards. The writer will coordinate cross-functional activities, mentor junior staff, and manage client relationships throughout the document development process.
The Senior Medical Writer will develop and manage high-quality clinical and regulatory documents, including protocols and clinical trial reports. They will also coordinate review cycles, ensure compliance with document lifecycle processes, and collaborate with cross-functional teams to meet project timelines.
The Medical Writer II is responsible for developing and managing high-quality clinical and regulatory documents, including protocols and clinical trial reports. They will coordinate review cycles, ensure document compliance, and collaborate with cross-functional teams to meet project timelines.
Acts as a lead medical writer responsible for preparing clinical study reports and protocols while ensuring compliance with SOPs and client requirements. Manages project timelines, budgets, and provides mentorship to junior staff while communicating directly with clients.
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.
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The Senior Medical Writer will create and manage clinical documents such as CTRs, CTPs, and IBs within a dedicated sponsor-aligned environment. They are responsible for overseeing document review cycles, ensuring compliance with SOPs, and collaborating with trial teams to meet project timelines.
The Principal Medical Writer leads the development of complex medical writing deliverables and manages documentation strategy across clinical studies. They also mentor junior staff, ensure compliance with regulatory standards, and collaborate with cross-functional teams to meet client objectives.
The Principal Medical Writer leads the development of complex clinical and regulatory documents while ensuring scientific accuracy and adherence to regulatory standards. They also manage document strategy, mentor junior staff, and collaborate with cross-functional teams to meet client objectives.
The Principal Medical Writer independently plans and prepares regulatory documents and medical communications to support product development. They are responsible for analyzing and presenting scientific and statistical information in compliance with ICH and regulatory guidelines.
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