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- Tasks: Translate complex scientific data into compelling 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 pharmaceutical industry.
- Qualifications: Bachelor's degree 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 TPBN1_UKTJ
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 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 but also demonstrate your commitment to staying updated in a rapidly evolving field.
✨Tip Number 2
Engage with professionals in the medical writing community through online forums or LinkedIn groups. Networking can provide valuable insights into the industry and may lead to referrals or recommendations for job openings.
✨Tip Number 3
Prepare to discuss specific examples of your previous work that showcase your ability to translate complex data into clear regulatory documents. Being able to articulate your experience will set you apart during interviews.
✨Tip Number 4
Highlight your collaborative skills by preparing examples of how you've successfully worked with cross-functional teams in the past. This is crucial for the role, as effective communication with various stakeholders is key to success.
We think you need these skills to ace 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'll be working on and the importance of compliance with European regulations.
Tailor Your CV: Customize your CV to highlight your relevant experience in regulatory writing and your knowledge of European regulations. Emphasize any specific projects or documents you've worked on that align with the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for medical writing and your understanding of the pharmaceutical industry. Mention your technical skills and how they will contribute to the team's success.
Highlight Collaboration Skills: In your application, emphasize your ability to work collaboratively with cross-functional teams. Provide examples of past experiences where your communication skills helped bridge gaps between different stakeholders.
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 stay updated on industry changes.
✨Demonstrate Technical Proficiency
During the interview, emphasize your ability to synthesize complex scientific data into clear and concise documents. Bring examples of your previous work that showcase your technical writing skills and attention to detail.
✨Highlight Collaborative Experiences
Since the role involves working with cross-functional teams, share examples of how you've effectively collaborated with different stakeholders. Discuss any challenges you faced and how you overcame them to foster productive partnerships.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to regulatory writing and their expectations for the role. This shows your genuine interest in the position and helps you assess if the company culture aligns with your values.
