27 Medical Writer jobs in United Kingdom 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 collaborate with internal and external stakeholders to develop publication plans, including manuscripts, abstracts, and posters. They are responsible for managing project timelines, leading meetings, and ensuring all deliverables adhere to industry standards and quality requirements.
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 Principal Medical Writer leads the development of high-quality regulatory and clinical documents while overseeing medical writing workstreams. They collaborate with cross-functional teams and mentor junior staff to ensure adherence to regulatory standards and project timelines.
The role involves leading the development of high-quality regulatory and clinical documents while coordinating assignments and timelines for medical writing projects. The writer will act as a key point of contact for clinical regulatory strategy and provide expert input for study designs and marketing applications.
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You will take ownership of high-complexity Phase II-IV clinical regulatory documents and manage the full document lifecycle from planning to delivery. This involves interpreting clinical data, authoring key regulatory content, and facilitating alignment across cross-functional teams.
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 deliver effective medical communication initiatives.
Manage end-to-end publication projects including manuscripts, abstracts, and posters while contributing to publication planning. Collaborate with cross-functional stakeholders and mentor junior writers to ensure scientific excellence and compliance with industry standards.
The Principal Medical Writer will lead complex, high-visibility publication projects while establishing credibility with senior stakeholders and key opinion leaders. They will also be responsible for mentoring junior writers, shaping team structure, and driving portfolio-level publication strategy.
The role involves creating high-quality medical education and medical affairs content, including clinical trial materials, slide decks, and patient-facing documents. You will also manage client relationships, review content from other writers, and identify opportunities for account growth.
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.
Lead the development and execution of medical writing strategies for clinical research projects, including CSRs, protocols, and pharmacometrics documents. Ensure all deliverables are inspection-ready, compliant with regulatory requirements, and effectively communicated to project teams.
The Associate Medical Writer supports the scientific services team by developing technical content such as manuscripts, slide decks, and digital materials. They also manage project timelines, perform data checking, and proactively research therapy areas to ensure high-quality scientific communication.
The Medical Writer will critically evaluate clinical literature and write complex regulatory documents such as protocols, investigator brochures, and clinical study reports. They will also manage project timelines, interact directly with clients, and mentor other team members.
The Medical Writer will critically evaluate and interpret medical literature to draft and edit various clinical development documents, including protocols and study reports. They will also manage project timelines, coordinate directly with clients, and mentor team members throughout the writing process.
The Principal Medical Writer will lead the production of scientifically accurate content across various formats while managing quality control and freelance writers. They will act as a trusted partner to clients, ensuring projects are delivered to deadline and budget while maintaining high scientific standards.
The Senior Medical Writer will produce high-quality, scientifically accurate content across various medical communications projects including medical affairs and educational materials. They will work independently to interrogate briefs, manage deadlines, and build strong relationships with agency and pharmaceutical clients.
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The Medical Writer II is responsible for developing and writing clinical trial documents, regulatory submissions, and scientific publications while ensuring accurate interpretation of clinical data. They also assist in managing medical writing resources and support business development activities through research and proposal writing.
Design and develop scientifically accurate medical materials such as slide decks, manuscripts, and website copy for various audiences. Manage client relationships, lead communications, and provide basic reviews and feedback to junior team members.
Lead the development, writing, and quality control of high-quality clinical study documents including protocols, IBs, and CSRs. Collaborate with sponsors and internal teams to ensure documents comply with regulatory guidelines and eCTD requirements.
Lead the development, writing, and QC review of high-quality clinical study documents including protocols, IBs, and CSRs. Ensure all documents comply with regulatory guidelines, SOPs, and eCTD requirements while collaborating with sponsors and internal teams.
Lead the planning, writing, and delivery of high-quality clinical and regulatory documents such as CSRs, protocols, and IBs. Provide subject matter expertise on document strategy and mentor junior medical writers to ensure operational excellence.
The Senior Medical Writer is responsible for developing high-quality clinical and regulatory documents such as study reports and protocols. They will collaborate with cross-functional teams and mentor junior writers to ensure compliance with regulatory standards.
Lead the delivery of medical communications projects, ensuring high-quality, on-time, and on-budget deliverables for clients. Manage and mentor junior medical writers while shaping client strategy and maintaining deep therapeutic area expertise.
Develop high-quality scientific content and partner with global clients on medical affairs and commercial strategies for neurologic diseases. The role also involves coaching junior writers and co-leading scientific meetings and client calls.
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.
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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.
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