Remote Medical Writer Jobs in United Kingdom

20 Medical Writer jobs in United Kingdom available for remote work from home. Apply for positions such as Medical Writer, Medical Writer, Principal Medical Writer- Clinical Focus and more! Discover the best work-from-home or hybrid, full- and part-time jobs.

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Remote Medical Writer Jobs in United Kingdom (20)

Search = Medical Writer Remote in = United Kingdom

Medical Writer

Lumanity · Full Time · 6 Days Ago
Lumanity
🌎 United Kingdom ⭐ 0-2 yrs exp πŸ’Ό Writing Medical Writer
Produce high-quality scientific content for medical communications projects including manuscripts, symposia, and advisory boards. Manage day-to-day client communications and stay updated on developments within assigned therapy areas.
Greenpark is hiring for remote Medical Writer

Medical Writer

Greenpark · Full Time · 12 Weeks Ago
Greenpark
🌎 United Kingdom ⭐ 2-5 yrs exp πŸ’Ό Writing Medical Writer
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.
Veristat is hiring for remote Principal Medical Writer- Clinical Focus

Principal Medical Writer- Clinical Focus

Veristat · Full Time · 14 hours ago
Veristat
🌎 France, Germany, Latvia, Spain, United Kingdom ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
The Principal Medical Writer plans and prepares regulatory documents and medical communications to support all phases of product development. They are responsible for analyzing and presenting scientific and statistical information in accordance with ICH and regulatory guidelines.

Associate Director, Medical Writer

MannKind Corporation · Full Time · 1 Week Ago
MannKind Corporation
🌎 United Kingdom πŸ’΅ $148K - $222K per year ⭐ 10+ yrs exp πŸ’Ό Writing Medical Writer
Lead the preparation and production of high-quality, ICH-compliant regulatory and scientific documents including protocols, CSRs, and submission documents. Coordinate cross-functional teams to ensure alignment with corporate milestones and maintain global regulatory compliance.

Principal Medical Writer

ICON plc · Full Time · 1 Week Ago
ICON plc
🌎 Spain, United Kingdom ⭐ 10+ yrs exp πŸ’Ό Writing Medical Writer
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.

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Senior Regulatory Medical Writer

Fortrea · Full Time · 1 Week Ago
Fortrea
🌎 Greece, Hungary, Portugal, United Kingdom ⭐ 2-5 yrs exp πŸ’Ό Legal Medical Writer
Lead the end-to-end development cycle of high-complexity Phase II-IV clinical regulatory documents for a leading pharma partner. Coordinate cross-functional teams to author protocols, IBs, and briefing packages while ensuring alignment with project strategy.

Lead Medical Writer

BOLDSCIENCE · Full Time · 2 Weeks Ago
BOLDSCIENCE
🌎 United Kingdom ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
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.

Senior Medical Writer

Nucleus Global · Full Time · 3 Weeks Ago
Nucleus Global
🌎 United Kingdom ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
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.
Veristat is hiring for remote Principal Medical Writer

Principal Medical Writer

Veristat · Full Time · 3 Weeks Ago
Veristat
🌎 France, Latvia, Spain, United Kingdom ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
The Principal Medical Writer plans and prepares regulatory documents and medical communications to support product development. This involves analyzing and presenting scientific and statistical information according to ICH and company standards.

Senior Medical Writer

Nucleus Global · Full Time · 3 Weeks Ago
Nucleus Global
🌎 United Kingdom ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
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.

Senior or Principal Medical Writer

ICON plc · Full Time · 5 Weeks Ago
ICON plc
🌎 Germany, Oman, Portugal, Romania, Spain, United Kingdom ⭐ 2-5 yrs exp πŸ’Ό Writing Medical Writer
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.

Senior Medical Writer

Theradex Oncology · Full Time · 6 Weeks Ago
Theradex Oncology
🌎 Denmark, Netherlands, Sweden, United Kingdom ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
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.

Principal Medical Writer

ICON plc · Full Time · 6 Weeks Ago
ICON plc
🌎 Oman, Romania, United Kingdom ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
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.
Veristat is hiring for remote Senior Medical Writer

Senior Medical Writer 14 APPLICANTS

Veristat · Full Time · 9 Weeks Ago
Veristat
🌎 France, Latvia, Spain, United Kingdom, United States ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
The Senior Medical Writer independently plans and prepares regulatory documents and medical communications to support product development phases. They are responsible for organizing, analyzing, and presenting scientific and statistical data in compliance with ICH and company standards.
Thermo Fisher Scientific is hiring for remote Senior Medical Writer - Non-Clinical

Senior Medical Writer - Non-Clinical 14 APPLICANTS

Thermo Fisher Scientific · Full Time · 11 Weeks Ago
Thermo Fisher Scientific
🌎 Bulgaria, Italy, Oman, Romania, Serbia, United Kingdom ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
The Senior Medical Writer will author and coordinate high-quality clinical and preclinical regulatory documents, including study reports and protocols. They will also provide mentorship to junior staff and collaborate with internal and external clients to ensure operational excellence.
Syneos Health is hiring for remote Sr. Medical Writer (Regulatory)

Sr. Medical Writer (Regulatory)

Syneos Health · Full Time · 11 Weeks Ago
Syneos Health
🌎 Canada, Norway, United Kingdom, United States πŸ’΅ $80600 - $145K per year ⭐ 5-10 yrs exp πŸ’Ό Legal Medical Writer
The Senior Medical Writer leads the preparation of complex regulatory documents, ensuring scientific accuracy and adherence to regulatory standards. They also coordinate cross-functional reviews and provide mentorship to less experienced team members.

Principal Medical Writer, Brand & Promotion

Precision Medicine Group · Full Time · 13 Weeks Ago
Precision Medicine Group
🌎 United Kingdom ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
The Principal Medical Writer is responsible for producing high-quality, evidence-based promotional content that aligns with brand strategy and adheres to the ABPI Code of Practice across various assets like campaigns, emails, and congress materials. This role involves leading content development, collaborating cross-functionally, acting as a client-facing scientific expert, and guiding the Medical-Legal-Regulatory (MLR) review process.

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Principal Medical Writer, Brand & Promotion

Precision AQ · Full Time · 13 Weeks Ago
Precision AQ
🌎 United Kingdom ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
The Principal Medical Writer is responsible for producing high-quality, evidence-based promotional content that aligns with brand strategy and adheres to the ABPI Code of Practice across various assets like campaigns, emails, and congress materials. This role involves leading content development, collaborating with cross-functional teams, acting as a client-facing scientific expert, and guiding the Medical-Legal-Regulatory (MLR) review process.
Syneos Health is hiring for remote Sr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; US/CAN
🌎 Canada, Norway, United Kingdom, United States πŸ’΅ $80600 - $145K per year ⭐ 5-10 yrs exp πŸ’Ό Legal Medical Writer
The role involves leading the clear and accurate completion of medical writing deliverables for studies, managing associated activities, and resolving client comments with minimal supervision. Responsibilities include completing various regulatory documents such as protocols, CSRs, IBs, submissions, and plain language summaries while adhering to regulatory standards and timelines.

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