The Associate Medical Writer is responsible for creating and formatting various medical documents while adhering to regulatory guidelines and QC processes. They will manage projects from start to finish, handle client feedback, and mitigate project risks.
Remote Medical Writer Jobs (102)
Search = Medical Writer
Develop and deliver high-quality scientific content for various materials, including manuscripts, congress materials, and interactive web projects. Lead projects by interpreting preclinical and clinical research data and providing editorial feedback to team members.
Lead and manage medical writing activities for clinical studies, including the development of manuscripts, abstracts, and posters. Coordinate with cross-functional teams to ensure scientific accuracy and adherence to regulatory standards and branding.
Lead the development and operational oversight of the company's scientific publications portfolio, including manuscripts, abstracts, and posters. Collaborate with cross-functional teams to translate complex genomic data into clear communications while ensuring adherence to ICMJE and GPP guidelines.
The role involves preparing high-quality medical imaging documentation, such as Site Imaging Manuals and Review Charters, to support clinical trials and regulatory submissions. The writer will collaborate with internal teams and sponsors to ensure accurate image acquisition and assessment criteria.
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Lead the development of high-quality clinical study documents, including protocols, IBs, and CSRs, ensuring compliance with regulatory guidelines. Manage the document lifecycle from template to final approval in collaboration with sponsors and internal teams.
Lead the development of high-quality clinical study documents, including protocols, IBs, and CSRs, ensuring compliance with regulatory guidelines. Manage the document lifecycle from template to final approval in collaboration with sponsors and internal teams.
Senior Medical Writer (Medical Information Writing)
Syneos Health
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Full Time
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2 Weeks Ago
Syneos Health
Lead and manage medical information writing projects, including the creation of global standard scientific response communications and FAQs. Mentor junior writers and collaborate with cross-functional teams to ensure scientific accuracy and regulatory compliance of deliverables.
Senior Medical Writer, Promotional Review
Thermo Fisher Scientific
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Full Time
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2 Weeks Ago
Thermo Fisher Scientific
Perform high-quality medical review of promotional and non-promotional materials to ensure clinical accuracy and compliance with FDA-OPDP requirements. Author medical information documents such as Standard Response Letters and FAQs while providing mentorship to junior writers.
The Senior Medical Writer designs and develops scientifically accurate materials such as slide decks, manuscripts, and website copy for various audiences. They manage client relationships, lead communications, and provide basic reviews and feedback to junior team members.
Responsible for managing the regulatory medical writing program to support the approval and licensure of medical devices in international markets. This includes writing and reviewing critical clinical regulatory documents such as CERs, CEPs, and PMCF reports in compliance with global requirements.
Lead the development and execution of medical writing strategies, including the preparation of clinical study protocols, reports, and regulatory submissions. Collaborate with cross-functional teams to analyze clinical trial data and mentor junior medical writers to ensure high-quality scientific documentation.
Responsible for preparing and reviewing clinical documents, including patient safety narratives and clinical study report appendices. The role involves supporting senior staff in drafting protocols and ensuring high-quality, timely delivery to sponsors.
Senior Medical Writer
Cactus Communications Services Pte. Ltd.
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Full Time
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3 Weeks Ago
Cactus Communications Services Pte. Ltd.
Develop and review high-quality medical communications deliverables including slide decks, manuscripts, and digital assets. Build strong relationships with clients and stakeholders while supporting business development through proposal creation.
The role involves researching, writing, and editing scientific manuscripts, abstracts, posters, and slide presentations for pharmaceutical clients. The writer must distill study data into high-quality deliverables while adhering to AMA style and good publication practices.
The role involves researching, writing, and editing scientific manuscripts, abstracts, posters, and slide presentations for pharmaceutical clients. The writer will collaborate with internal teams to distill study data into high-quality deliverables following AMA style.
Develop high-quality scientific content including publications, slide sets, and training materials using AI-enabled workflows. Collaborate with internal teams and clients to ensure materials are strategically aligned and scientifically rigorous.
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Medical Writer - Scientific Communications Specialist - (English)
Med Communications International
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Full Time
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3 Weeks Ago
Med Communications International
Develop and review scientifically accurate content for medical documents, slide decks, and manuscripts while ensuring alignment with regulatory guidelines. Provide medical information support to healthcare professionals and internal stakeholders to support brand objectives.
Senior/Principal Medical Writer
Trilogy Writing and Consulting
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Full Time
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3 Weeks Ago
Trilogy Writing and Consulting
Lead the preparation of various clinical regulatory documents and scientific publications in collaboration with client authoring teams. Manage project timelines, budgets, and review cycles while overseeing other writers and QC specialists.
Lead the preparation and editing of clinical study documents, including protocols, CSRs, and regulatory submissions. Collaborate with cross-functional teams to analyze clinical trial data and mentor junior medical writers.
The Principal Medical Writer will collaborate with teams to create and manage publications that support drug development and commercialization. They will apply their expertise to understand customer needs and shape solutions accordingly.
The Senior Medical Writer leads the completion of medical writing deliverables, ensuring clarity and accuracy in scientific information. They manage writing activities across studies and coordinate with various departments while adhering to regulatory standards.
The Senior Medical Writer is responsible for preparing critical regulatory documents including IND applications, clinical study protocols, and investigator's brochures for oncology trials. The role involves collaborating directly with clients, medical monitors, and senior leadership to manage document timelines and review cycles.
Leads the creation and accurate completion of various medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinates with cross-functional teams and clients to ensure scientific clarity and adherence to regulatory standards.
Develop and manage high-quality clinical and regulatory documents to ensure compliance with EU MDR and FDA standards. Plan and report clinical data collection for Post-Market Clinical Follow-up and clinical trials.
Create and edit high-quality publications and materials focused on patient safety and risk management for healthcare providers and the public. Manage digital content, social media campaigns, and editorial calendars while collaborating with internal stakeholders.
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Lead the development of high-quality regulatory and clinical documents to support submissions to global regulatory authorities. Manage medical writing projects, including timeline development and cross-functional coordination to ensure compliance with industry standards.
Lead the development of high-quality regulatory and clinical documents to support client submissions to regulatory authorities. Coordinate writing assignments, formulate strategies, and provide functional guidance on international regulatory requirements.
Principal Medical Writer
4D Molecular Therapeutics
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Full Time
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5 Weeks Ago
4D Molecular Therapeutics
The Principal Medical Writer will lead the planning, development, and execution of high-quality clinical and regulatory documents, specifically focusing on BLA-enabling activities for late-stage gene therapy programs. This role involves coordinating internal and external writing resources while ensuring scientific accuracy and alignment with global regulatory standards.
The Medical Writer is responsible for the development, scientific integrity, and accuracy of medical content for pharmaceutical and medical device clients. They collaborate with cross-functional teams to execute deliverables while ensuring alignment with regulatory, compliance, and client standards.
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