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Salary:
- 55.96 - 67.16 per hour PAYE or 75-90 per hour Ltd/Umbrella (outside IR35)
- You will manage the preparation, review, and submission of nonclinical summary documents for both early development and marketing applications
- You will work with regulatory and scientific functions to ensure comprehensive and accurate nonclinical dossiers are being submitted to HAs.
- Working closely with Nonclinical Project Leaders and Scientists in composing regulatory submission documents, study reports and other research-related documents
- You will develop and maintain processes, tools, and guidelines enabling high-quality document production
- You hold a university degree in a life science.
- You have several years of working experience in scientific writing and editing in a nonclinical, regulatory domain.
- You have an excellent command of writing and editing software, with an interest in exploring and integrating new tools and technologies.
- You build a culture of trust around you and are comfortable working with a wide array of stakeholders.
- You are obsessed with meeting customer needs and thus, high-quality documentation.
- You take ownership of your work and are proactive in taking action to resolve issues.
- Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.
- This role can be remote or hybrid, based at our clients site in Welwyn Garden City.
- For more information, or to apply for this Regulatory Scientific Writer please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only).
Please note:This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
