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- Tasks: Transform complex scientific data into clear regulatory documents.
- Company: Join a dynamic medical communications agency focused on pharmaceutical excellence.
- Benefits: Enjoy competitive pay, flexible remote work, and professional growth opportunities.
- Why this job: Be part of a collaborative team making an impact in the healthcare industry.
- Qualifications: Bachelor's in a scientific field and experience in regulatory writing required.
- Other info: Full or part-time positions available; extensive training provided.
The predicted salary is between 43200 - 72000 £ per year.
About Us: We are a dynamic and growing medical communications agency committed to excellence in pharmaceutical communications. As we expand our regulatory department, we are actively seeking a talented and experienced European Senior Regulatory Writer to join our team. Role Overview: As a Senior Regulatory Writer, you will play a key role in translating complex scientific and clinical data into compelling regulatory documents. Your expertise will be crucial in ensuring compliance with European regulations and industry standards. Fully remote, home based. Key Responsibilities: Regulatory Expertise: Leverage your in-depth knowledge of European regulations to contribute to the development of high-quality regulatory documents, including but not limited to clinical study reports, regulatory submissions, protocols, investigator brochures, and marketing authorisation applications. Extensive training is offered for documents you do not currently have experience in. Technical Excellence: Dive into the technical details of scientific and clinical data, demonstrating a keen ability to synthesize and present information accurately and coherently. Stay abreast of industry advancements and regulatory updates to ensure the highest standards of technical accuracy. Collaborative Engagement: Work collaboratively with cross-functional sponsor teams, bridging the gap between regulatory affairs, clinical teams, and other stakeholders. Your effective communication skills will be instrumental in fostering productive partnerships. Flexible Working Arrangements: Remote Accessibility: Embrace the opportunity to work remotely, allowing you to cultivate a conducive work environment that optimizes your productivity and work-life balance. Full or part-time: We are happy to consider writers for either part or full time working Qualifications and Experience: Bachelor’s degree in a relevant scientific discipline. Proven experience in regulatory writing, with a focus on European regulations. Strong technical acumen with the ability to comprehend and articulate complex scientific and clinical information. Benefits: Competitive compensation package reflective of your skills and expertise. Opportunity for professional growth within a thriving SME environment. Flexible working arrangements to accommodate your unique work style. How to Apply: Please apply directly through this advert, reach out to Vivify Talent via our website (vivifytalent.com) or on +44 (0) 1223 080 457 JBRP1_UKTJ
Vivify Talent Limited | Senior Medical Writer employer: Vivify Talent Limited
Contact Detail:
Vivify Talent Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Vivify Talent Limited | Senior Medical Writer
✨Tip Number 1
Familiarize yourself with the latest European regulations and guidelines related to regulatory writing. This knowledge will not only boost your confidence during interviews but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Highlight any experience you have working collaboratively with cross-functional teams. Be prepared to share specific examples of how you've effectively communicated complex information to different stakeholders, as this is crucial for the role.
✨Tip Number 3
Showcase your technical writing skills by preparing a portfolio of relevant documents you've created in the past. Even if they are not regulatory documents, demonstrating your ability to synthesize and present scientific data clearly can set you apart.
✨Tip Number 4
Since the position is fully remote, emphasize your ability to work independently and manage your time effectively. Share examples of how you've successfully navigated remote work challenges in the past to reassure them of your adaptability.
We think you need these skills to ace Vivify Talent Limited | Senior Medical Writer
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Senior Regulatory Writer. Familiarize yourself with the types of documents you will be expected to produce and the European regulations that govern them.
Tailor Your CV: Customize your CV to highlight your relevant experience in regulatory writing and your knowledge of European regulations. Be specific about your past roles and how they relate to the job description provided by Vivify Talent Limited.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for medical writing and your understanding of the pharmaceutical industry. Mention any specific experiences that demonstrate your ability to translate complex scientific data into clear regulatory documents.
Highlight Collaboration Skills: Since the role involves working with cross-functional teams, emphasize your collaborative skills in both your CV and cover letter. Provide examples of how you've successfully worked with different stakeholders in previous positions.
How to prepare for a job interview at Vivify Talent Limited
✨Showcase Your Regulatory Knowledge
Be prepared to discuss your understanding of European regulations in detail. Highlight specific experiences where you successfully navigated regulatory requirements, and be ready to explain how you would apply this knowledge in the role.
✨Demonstrate Technical Proficiency
Since the role requires a strong grasp of scientific and clinical data, come equipped with examples of documents you've written or contributed to. Discuss how you ensure accuracy and clarity in your writing, and stay updated on industry advancements.
✨Emphasize Collaboration Skills
This position involves working with cross-functional teams, so share examples of how you've effectively communicated and collaborated with different stakeholders. Highlight any experience you have in bridging gaps between regulatory affairs and clinical teams.
✨Prepare for Remote Work Dynamics
As the role is fully remote, be ready to discuss how you manage your time and productivity while working from home. Share strategies that help you maintain a work-life balance and ensure effective communication with your team.
