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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 fully remote work and extensive training opportunities.
- Why this job: Make an impact in the pharmaceutical industry while working with a collaborative team.
- Qualifications: Experience in regulatory writing and knowledge of European regulations required.
- Other info: Opportunity for growth in a rapidly expanding department.
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 a…
Senior Regulatory Writer employer: Vivify Talent
Contact Detail:
Vivify Talent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory Writer
✨Tip Number 1
Familiarize yourself with the latest European regulations and guidelines relevant to regulatory writing. This knowledge will not only boost your confidence but also demonstrate your commitment to staying updated in a fast-evolving field.
✨Tip Number 2
Network with professionals in the medical communications and regulatory writing fields. Engaging with industry peers can provide valuable insights and potentially lead to referrals or recommendations for job openings.
✨Tip Number 3
Showcase your ability to translate complex scientific data into clear, concise documents. Prepare examples of your previous work that highlight your technical writing skills and your understanding of regulatory requirements.
✨Tip Number 4
Be proactive in seeking out additional training opportunities related to regulatory writing. This could include online courses or workshops that focus on specific types of regulatory documents you may not have experience with yet.
We think you need these skills to ace Senior Regulatory Writer
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Senior Regulatory Writer position. Understand the key responsibilities and required skills, especially the importance of European regulatory knowledge.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience with regulatory documents and any specific knowledge of European regulations. Provide examples of past work that demonstrate your ability to translate complex data into clear regulatory submissions.
Showcase Technical Skills: Detail your technical writing skills and familiarity with scientific and clinical data. Mention any relevant software or tools you are proficient in that can aid in document preparation.
Tailor Your Application: Customize your application materials to reflect the values and mission of the medical communications agency. Show your enthusiasm for the role and how your background aligns with their commitment to excellence in pharmaceutical communications.
How to prepare for a job interview at Vivify Talent
✨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 Writing Skills
Bring samples of your previous regulatory documents to the interview. This will allow you to showcase your ability to translate complex scientific data into clear and compelling narratives, which is crucial for the Senior Regulatory Writer position.
✨Emphasize Collaboration Experience
Since the role involves working with cross-functional teams, share examples of how you've effectively collaborated with different stakeholders in past projects. Discuss how you bridged gaps between regulatory and clinical teams to achieve successful outcomes.
✨Stay Updated on Industry Trends
Research recent changes in European regulations and industry standards before your interview. Being knowledgeable about current trends will demonstrate your commitment to the field and your proactive approach to staying informed.
