141 Regulatory Writing jobs in the United Kingdom

We are looking for an experienced Regulatory/Medical Writer who is ready to step into a more consultative, client-facing role . While you’ll bring deep hands-on expertise in regulatory document authorship, this position is focused less on day-to-day writing and more on guiding clients, providing best-practice recommendations, and ensuring the strategic and compliant delivery of high-quality regulatory documents.

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.

We are looking for an experienced Regulatory/Medical Writer who is ready to step into a more consultative, client-facing role . While you’ll bring deep hands-on expertise in regulatory document authorship, this position is focused less on day-to-day writing and more on guiding clients, providing best-practice recommendations, and ensuring the strategic and compliant delivery of high-quality regulatory documents.

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.

We are looking for an experienced Regulatory/Medical Writer who is ready to step into a more consultative, client-facing role . While you’ll bring deep hands-on expertise in regulatory document authorship, this position is focused less on day-to-day writing and more on guiding clients, providing best-practice recommendations, and ensuring the strategic and compliant delivery of high-quality regulatory documents.

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.

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.

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.