Senior Regulatory Writer

5 days ago


London, United Kingdom X4 Group Full time

An independent pharmaceutical consultancy is seeking a Senior Regulatory Writers to support the Directors in leading the regulatory writing department.

**Senior Regulatory Writer Role:**
- Lead the preparation of clinical and regulatory documents: Protocols, Clinical Study Reports (CSRs), Investigator’s Brochures (IBs), Integrated Safety and Efficacy Summaries, Subject Consent Forms, Briefing Documents, Clinical Overviews, RMPs etc.
- Work as part of a team to deliver projects in line with budgets and timelines.
- Ensure high standards of quality on all documentation.

**Senior Medical Writer Requirements**:

- Minimum 3 years of industry regulatory writing experience.
- Varied therapeutic area background.
- Highly proficient with styles of writing for various regulatory documents
- Excellent understanding of industry regulations, Good Clinical Practices, and ICH guidelines
- Masters or PhD in scientific, medical, clinical discipline preferred.

In return, you will be offered a starting salary of £45,000 - £55,000 per annum.

If this role is not what you are looking for don't worry. At X4 Communications we cover all permanent and contract positions, with specialist industry sector teams. You can check out all of our roles on our website and sign up for job alerts so you are thefirst to know about a new opportunity.



  • London, Greater London, United Kingdom RBW Consulting Full time

    Job Title: Senior Regulatory WriterThis role is responsible for preparing and submitting high-quality CMC regulatory documents to support registration activities for both small molecule and biopharmaceutical therapeutic assets. The ideal candidate will have a strong background in CMC regulatory science, technical writing skills, and experience in managing...


  • London, Greater London, United Kingdom Albion Rye Associates Full time

    **Job Overview:**We are seeking an experienced Senior Regulatory Writer to join our team at Albion Rye Associates. This role offers the opportunity to work on key drug development projects for biopharmaceutical companies, making a significant impact in helping critical drug products reach patients.Key Responsibilities:Prepare high-quality documentation for...


  • London, United Kingdom CV-Library Full time

    Senior CMC Regulatory Technical Writer Are you a detail-oriented technical writer with a passion for regulatory science? Join a dynamic CMC Regulatory Department as a Senior CMC Regulatory Technical Writer. In this pivotal role, you will be instrumental in preparing and submitting high-quality CMC regulatory documents to support registration activities for...


  • London, United Kingdom RBW Consulting Full time

    Senior CMC Regulatory Technical Writer Are you a detail-oriented technical writer with a passion for regulatory science? Join a dynamic CMC Regulatory Department as a Senior CMC Regulatory Technical Writer. In this pivotal role, you will be instrumental in preparing and submitting high-quality CMC regulatory documents to support registration activities for...


  • London, Greater London, United Kingdom Barrington James Full time

    Job Title: Lead Regulatory WriterBarrington James is seeking a highly skilled Lead Regulatory Writer to join our Medical Writing and Regulatory Affairs department. As a senior leader, you will be responsible for overseeing the preparation and delivery of high-quality regulatory submissions and medical writing outputs.With a strong background in medical...


  • London, Greater London, United Kingdom Publicis Groupe Holdings B.V Full time

    In the role of Regulatory Medical Writer at Publicis Groupe Holdings B.V, you will be responsible for developing accurate and engaging content for medical education materials while adhering to regulatory requirements. Strong communication skills and the ability to collaborate with clients and senior writers are essential for success in this position....


  • London, Greater London, United Kingdom Richmond Pharmacology Full time

    Role and ResponsibilitiesRichmond Pharmacology is seeking a skilled Medical Writer to join our team in London Bridge. The successful candidate will have excellent written and verbal communication skills, with the ability to craft high-quality, scientifically accurate medical and scientific communications. You will be comfortable working independently and...

  • Regulatory Writer

    4 days ago


    London, Greater London, United Kingdom RBW Consulting Full time

    Overview:RBW Consulting seeks a skilled Senior CMC Regulatory Technical Writer to prepare and submit high-quality regulatory documents. This is a freelance position with potential for renewal.About the Role:Prepare, review, and finalize CMC regulatory submission documents for late-stage clinical applications (Phase 3) and marketing applications.Develop and...


  • London, United Kingdom VRS Regulatory Full time

    An excellent opportunity for established or aspiring chemical regulatory professionals to join a leading EU chemicals risk management and policy consultancy. You will use your chemical regulatory science knowledge alongside economists and social scientists on a wide range of multi-disciplinary projects including REACH compliance, authorisations,...


  • London, United Kingdom Writer Full time

    **About Writer** AI your people will love. That's our vision, and it contains multitudes: - ) - AI_ - your people_ - will love._ We're filling a big need for generative AI built ground-up for the needs of enterprises and embraced by their teams. As generative AI became a board-level initiative almost overnight for most enterprises, our market matured...


  • London, United Kingdom X4 Group Full time

    **The Company:** An international consultancy with offices in the UK, US and across Europe, recently became part of a large group of companies with a global outreach. Focused on providing highly specialised Medical Writing services to Pharmaceutical, Biotech and MedicalDevice clients. **Freelance Regulatory Writer Role:** - Prepare clinical and regulatory...


  • London, United Kingdom X4 Group Full time

    **The Company:** An international consultancy with offices in the UK, US and across Europe, recently became part of a large group of companies with a global reach in the pharmaceutical industry. Focused on providing highly specialised Medical Writing services to Pharmaceutical,Biotech and Medical Device clients. **Freelance Regulatory Writer Role:** -...


  • London, Greater London, United Kingdom Writer Full time

    We are seeking a highly skilled Senior Customer Success Leader to join our team at Writer. As a key member of our customer success organization, you will be responsible for driving business growth and ensuring the successful adoption of our platform by Fortune 50-100 accounts.Job OverviewThe successful candidate will have 7+ years of experience in a CSM role...


  • London, Greater London, United Kingdom RBW Consulting Full time

    About the RoleWe are seeking a Senior CMC Regulatory Technical Writer to join our dynamic CMC Regulatory Department. In this pivotal role, you will be instrumental in preparing and submitting high-quality CMC regulatory documents to support registration activities for both small molecule and biopharmaceutical therapeutic assets.Main Tasks and...


  • London, Greater London, United Kingdom MMS Holdings Inc Full time

    Job Title: Regulatory Medical WriterAbout MMS Holdings Inc.MMS Holdings Inc. is a leading Contract Research Organization (CRO) providing innovative data-focused services to the pharmaceutical, biotech, and medical device industries. Our scientific approach and technology-enabled services enable us to support complex trial data and regulatory submission...


  • London, Greater London, United Kingdom writer Full time

    Solution Delivery ManagerWe are looking for a Senior Manager Solution Delivery to join our team at Writer. In this role, you will be responsible for transforming our approach to facilitating customer evaluations and proofs of concept, empowering our partners through onboarding, education, and strategy development, and collaborating with SAs and the extended...


  • London, United Kingdom X4 Group Full time

    Join an international regulatory consultancy as a Senior Medical Writer and support the Head of Department in creating a broad range clinical and regulatory documents for global submissions. **The Company:** **Senior Medical Writer Responsibilities:** - Create and update regulatory documentation for submission to regulatory authorities according to...


  • London, Greater London, United Kingdom Writer Full time

    Company OverviewAbout Writer:Writer is the pioneering full-stack generative AI platform that empowers leading enterprises to unlock transformative ROI. As a company founded in 2020 with hubs in San Francisco, New York City, Austin, Chicago, and London, we've grown to a team of over 250 employees driven by innovation and speed.We're on a mission to create a...


  • London, United Kingdom Writer Full time

    Writer is the full-stack generative AI platform delivering transformative ROI for the world's leading enterprises. Magazine, Writer empowers hundreds of customers like Accenture, Intuit, L'Oreal, Mars, Salesforce, and Vanguard to transform the way they work. Our suite of development tools is powered by Palmyra - Writer's state-of-the-art family of LLMs -...


  • London, Greater London, United Kingdom Vivify Talent Limited Full time

    About the CompanyVivify Talent Limited is a nimble regulatory writing consultancy that values passion, science, and writing. We're passionate about helping professionals achieve their goals and grow in their careers.Job SummaryWe're seeking a dynamic Senior Regulatory Writer to spearhead key documents and projects. The ideal candidate will have excellent...