29 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 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 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 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 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.
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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.
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.
Leads the preparation and completion of complex clinical medical writing deliverables while ensuring scientific accuracy and regulatory compliance. Coordinates cross-functional activities and provides mentorship to less experienced writers to ensure projects are delivered on time and within budget.
The Senior Medical Writer will produce high-quality scientific content for various medical communications projects while managing client relationships and expectations. They are responsible for developing content with minimal supervision and ensuring all work aligns with client strategy and budget requirements.
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.
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Leads the creation and accurate completion of regulatory medical writing deliverables, including protocols, clinical study reports, and NDA submissions. Coordinates with cross-functional teams and clients to ensure documents meet regulatory standards and are delivered on time and budget.
Develop and deliver high-quality publication content, including manuscripts and posters, for a significant rare disease account. Contribute to publication strategy and build long-term relationships with clients and medical experts.
Lead the production of high-quality medical publications, abstracts, and posters from conception to completion. Act as the primary contact for clients and provide senior review, training, and mentorship to other writers.
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.
The Senior Medical Writer authors critical regulatory documents including clinical study reports, protocols, and investigator brochures. They collaborate with clinical teams and biostatisticians to synthesize complex data into clear prose and mentor junior writing staff.
Lead the development of high-quality regulatory and clinical documents, including clinical study reports and protocols. Oversee medical writing workstreams and mentor junior writers to ensure adherence to industry standards and timelines.
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 lead publications and medical affairs strategies for global oncology clients. Mentor junior medical writers and maintain strong relationships with clients and authors.
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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.
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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