Explore regulatory writing opportunities that demand precision and expertise. These roles involve crafting clear, concise, and compliant documentation for various industries, including pharmaceuticals, 145 Regulatory Writing jobs in the United Kingdom
Medical Writer - Medical Communications
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Medical Writer – Medical Communications
Find out more about the daily tasks, overall responsibilities, and required experience for this opportunity by scrolling down now.Position: Medical Writer (medical affairs)
Location: London (2 days in the office)
Contract Type: Permanent
Salary: Up to £46k
Start: ASAP
Medical Writer:
This is an excellent opportunity to join a flourishing Editorial team! As a member of the scientific team, you will have the chance to shape your role to fit your strengths and be instrumental in the ongoing development and growth of the division.
The successful candidate will have the opportunity to work on a range of projects across the full spectrum of medical communications activities, including congress activities, advisory boards, symposia, training materials, websites, and digital apps. Some of the key therapy areas include oncology, rare diseases, cardiovascular and obesity.
With a vibrant and sociable team environment, modern offices in London, intensive on-the-job coaching, and a program of targeted training supplemented by an excellent benefits package, our client values the difference in their employees and puts a strong emphasis on creating opportunities for advancement that complement and develop strengths and further careers.
Role & Responsibilities:
- Provide high-level medical writing support within accounts, achieving writing excellence across therapy areas and the communication mix and target audiences
- Review written scientific documents for writing style, strategy, content accuracy and fact/data checking, and provide constructive feedback, in addition to ensuring scientific accuracy
- Act as the Technical Lead on designated client projects
- Apply expertise and broad experience of medical communications to the development of strategic communications programmes across accounts
- Ensure all assigned projects are delivered to the highest possible editorial and scientific standards, to deadline and within budget
- Develop and maintain strong working relationships with clients and external thought leaders
- Manage and monitor own workload and that of junior writers assigned to projects. Monitor project budgets. Anticipate and provide solutions to budget and/or resource needs or limitations. Identify where new processes may be required and support their development
- Keep up to date with industry codes of practice/legislation and external issues or events that may affect existing accounts
- Monitor project costs against agreed budgets and notify the Client Services team of any changes to specification at the earliest opportunity
- Contribute to the development of account plan forecasts in liaison with client services leads
- Research and contribute to the writing and review of new business proposals and pitch presentations, playing a central role from initial strategic brainstorming to proposal delivery
- Proactively identify possible new business opportunities within assigned accounts
Requirements:
- Degree (science, preferably life science); PhD or MSc (desirable)
- Scientific knowledge and understanding
- Proficiency in delivering high-quality written work
- Presentation skills
- Able to attend international events
- High level of drive, motivation, and initiative
- Excellent communication and interpersonal skills
- Awareness of industry guidelines and best practice and their application
- 2+ years of experience working in Medical Communications (agency)
#medcomms #medicalcommunications #medicalwriter #medicaleducation #healthcareadvertising #healthcare #pharma
Medical Writer – Medical Communications
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What you’ll do
- Act as a trusted advisor to clients on regulatory writing deliverables, offering guidance on structure, compliance, and best practices.
- Oversee and review a broad range of documents (e.g., CSRs, IBs, PLSs ) to ensure alignment with ICH/GxP/GPP standards.
- Partner closely with client teams, offering scientific and regulatory insight that adds value beyond document production.
- Mentor and collaborate with writing teams, leveraging your background to ensure accuracy, clarity, and regulatory compliance.
- Represent the writing function confidently in meetings, workshops, and client interactions.
What we’re looking for
- Strong background as a medical/regulatory writer within pharmaceutical companies, CROs, or regulatory service providers .
- Proven familiarity with regulatory guidelines (ICH, GxP, GPP) and regulated deliverables (CSRs, IBs, PLSs).
- Excellent communication skills, with the ability to translate technical writing expertise into client-facing consulting .
- A detail-oriented, organized professional who can balance writing quality with broader consulting impact.
- Experience in scientific communications a plus, but regulatory writing expertise is essential.
Why join us?
This is a unique opportunity for a writer who wants to evolve into a strategic, consultative role . You’ll still leverage your writing background every day, but instead of focusing on drafting, you’ll guide clients, shape deliverables, and influence best practices in regulatory writing.
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What you’ll do
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- Partner closely with client teams, offering scientific and regulatory insight that adds value beyond document production.
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- Excellent communication skills, with the ability to translate technical writing expertise into client-facing consulting .
- A detail-oriented, organized professional who can balance writing quality with broader consulting impact.
- Experience in scientific communications a plus, but regulatory writing expertise is essential.
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Regulatory Writing Submission Graduate
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Regulatory Writing Submission Graduate
Posted 8 days ago
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Location: White City, London
Pay Rate: £31,050
12 Month Fixed Term Contract
Hybrid Working Scheme - 2/3 days on site per week
About the Role
We’re looking for a detail-oriented and scientifically driven Regulatory Writing Submissions Graduate to join our clients Regulatory Writing & Submissions (RWS) team. In this role, you’ll contribute to the creation of high-quality clinical and safety documentation that supports global drug development and regulatory submissions.
Key Responsibilities
- Draft and edit clinical and safety documents under guidance, including:
- Clinical Study Protocols (CSPs) and amendments
- Non-registration Clinical Study Reports (CSRs)
- Development Safety Update Reports (DSURs)
- Clinical Trial Registration Documents
- Represent RWS in Clinical Trial Teams (CTTs)
- Support planning of data analyses and presentation for CSRs
- Ensure documentation complies with internal standards and regulatory guidelines
- Liaise with publishing teams to ensure timely delivery of final documents
- Contribute to process improvements within RWS
- Maintain compliance with audits, SOPs, and training requirements
What Success Looks Like
- Timely delivery of high-quality documents that meet internal and external standards
- Completion of a meaningful volume of work annually, aligned with performance metrics
Qualifications & Experience
Education:
- Minimum: University degree in life sciences or equivalent
- Preferred: Advanced degree in life sciences or healthcare
Experience:
- Some experience in medical writing or relevant pharmaceutical industry roles
- Solid understanding of global regulatory processes and documentation
- Familiarity with biostatistics principles
- Strong problem-solving and project management skills
- Excellent written and verbal communication skills
- Ability to work in a matrixed, cross-cultural environment
Why Join Us?
This is a fantastic opportunity to grow your career in regulatory writing within a collaborative and globally connected team. You’ll be at the forefront of clinical documentation, helping bring innovative therapies to patients worldwide.
Regulatory Writing Submission Graduate
Posted 8 days ago
Job Viewed
Job Description
Location: White City, London
Pay Rate: £31,050
12 Month Fixed Term Contract
Hybrid Working Scheme - 2/3 days on site per week
About the Role
We’re looking for a detail-oriented and scientifically driven Regulatory Writing Submissions Graduate to join our clients Regulatory Writing & Submissions (RWS) team. In this role, you’ll contribute to the creation of high-quality clinical and safety documentation that supports global drug development and regulatory submissions.
Key Responsibilities
- Draft and edit clinical and safety documents under guidance, including:
- Clinical Study Protocols (CSPs) and amendments
- Non-registration Clinical Study Reports (CSRs)
- Development Safety Update Reports (DSURs)
- Clinical Trial Registration Documents
- Represent RWS in Clinical Trial Teams (CTTs)
- Support planning of data analyses and presentation for CSRs
- Ensure documentation complies with internal standards and regulatory guidelines
- Liaise with publishing teams to ensure timely delivery of final documents
- Contribute to process improvements within RWS
- Maintain compliance with audits, SOPs, and training requirements
What Success Looks Like
- Timely delivery of high-quality documents that meet internal and external standards
- Completion of a meaningful volume of work annually, aligned with performance metrics
Qualifications & Experience
Education:
- Minimum: University degree in life sciences or equivalent
- Preferred: Advanced degree in life sciences or healthcare
Experience:
- Some experience in medical writing or relevant pharmaceutical industry roles
- Solid understanding of global regulatory processes and documentation
- Familiarity with biostatistics principles
- Strong problem-solving and project management skills
- Excellent written and verbal communication skills
- Ability to work in a matrixed, cross-cultural environment
Why Join Us?
This is a fantastic opportunity to grow your career in regulatory writing within a collaborative and globally connected team. You’ll be at the forefront of clinical documentation, helping bring innovative therapies to patients worldwide.