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- Tasks: Write and edit clinical regulatory documents while mentoring a dynamic team.
- Company: Top medical devices company with a focus on innovation and research.
- Benefits: Competitive salary, professional growth, and fully remote work options.
- Why this job: Join a stimulating environment at the forefront of medical research and make a real impact.
- Qualifications: PhD/PharmD or Master's in life sciences with relevant experience.
- Other info: Exciting one-year contract with opportunities for career advancement.
The predicted salary is between 36000 - 60000 £ per year.
Are you an experienced regulatory affairs writer looking for a new challenge? Our client, a top medical devices company, is seeking a Senior Regulatory Affairs Writer to join their dynamic team. This role offers a stimulating work environment at the forefront of medical research, along with ample opportunities for professional growth and development. It’s fully remote, allowing you to work from anywhere in the UK, Israel, or Germany.
Responsibilities:
- Write and/or edit various clinical regulatory documents: You will be responsible for writing and editing a wide range of clinical regulatory documents, including CSRs, IBs, Protocols, Summaries, Briefing Books, Pediatric Plans, and Model 2 summaries for submissions. Your expertise in driving project consensus and foreseeing potential issues will be highly valued.
- Oversee and mentor: Take on a leadership role and oversee outsourced writing deliverables. Provide guidance, support, and strategic assistance to the team. You’ll be responsible for ensuring that clinical documents are accurate, complete, and adhere to regulatory guidelines and company standards.
- Collaborate and communicate: Be a clear communicator and a team player. You’ll work in a cross-functional environment, collaborating with various teams and stakeholders. Your ability to effectively communicate and drive project consensus will be key to your success in this role.
Requirements:
- Life sciences background: A PhD/PharmD in life sciences (or related field) with a minimum of 5 years of experience, or a Master’s degree in life sciences (or related field) with a minimum of 7 years of experience.
- Willingness to learn and grow: Our client is looking for a motivated candidate who is eager to learn and grow as part of a team. While extensive experience is not required, a willingness to continuously develop your skills and contribute to the team’s success is essential.
- Problem-solving skills: You’ll need to be a proactive problem solver. Your ability to anticipate issues, drive project consensus, and find solutions will be crucial in this role.
Benefits:
- Competitive compensation package: Our client understands the value of your skills and expertise. They offer a highly competitive compensation package that reflects your experience and contribution.
- Professional growth and development: You’ll have the opportunity to work on a diverse range of projects, from writing and editing clinical regulatory documents to providing oversight for outsourced deliverables. You’ll be able to enhance your skills and broaden your knowledge in the field of medical research.
- Stimulating work environment: Join a team at the forefront of medical research, where every day brings new challenges and opportunities to make a difference. Collaborate with cross-functional teams and contribute to the development of crucial clinical regulatory documents that impact the advancement of medical science.
Apply now and become a part of this exciting journey!
Sr. Regulatory Affairs Writer, Remote in the UKNonStop Consulting in England employer: NonStop Consulting
Contact Detail:
NonStop Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Sr. Regulatory Affairs Writer, Remote in the UKNonStop Consulting in England
✨Tip Number 1
Network like a pro! Reach out to your connections in the regulatory affairs field and let them know you’re on the lookout for new opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Get your online presence sorted! Make sure your LinkedIn profile is up-to-date and showcases your skills as a Senior Regulatory Affairs Writer. Engage with relevant content and connect with industry professionals to boost your visibility.
✨Tip Number 3
Practice your interview skills! Prepare for common questions related to regulatory writing and be ready to discuss your problem-solving abilities. Mock interviews with friends or mentors can help you feel more confident.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of exciting roles, including this one, and applying directly can give you an edge. Plus, it’s super easy to keep track of your applications!
We think you need these skills to ace Sr. Regulatory Affairs Writer, Remote in the UKNonStop Consulting in England
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the role of Senior Regulatory Affairs Writer. Highlight your relevant experience in writing clinical regulatory documents and any leadership roles you've taken on. We want to see how your background aligns with what our client is looking for!
Showcase Your Problem-Solving Skills: In your application, don’t forget to mention specific examples where you’ve anticipated issues and found solutions. This is key for the role, so let us know how you’ve tackled challenges in the past!
Be Clear and Concise: When writing your application, clarity is crucial. Use straightforward language and get to the point quickly. We appreciate a well-structured application that’s easy to read and understand.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of applications and ensures you don’t miss out on this exciting opportunity. Let’s get your career moving!
How to prepare for a job interview at NonStop Consulting
✨Know Your Documents Inside Out
As a Senior Regulatory Affairs Writer, you'll be dealing with various clinical regulatory documents. Make sure you familiarise yourself with the types of documents mentioned in the job description, like CSRs and IBs. Being able to discuss these confidently will show your expertise and readiness for the role.
✨Showcase Your Leadership Skills
Since this role involves overseeing and mentoring others, prepare examples of how you've successfully led projects or teams in the past. Highlight your ability to provide guidance and support, as well as how you’ve ensured accuracy and adherence to regulatory guidelines.
✨Demonstrate Your Problem-Solving Abilities
The job requires proactive problem-solving skills. Think of specific instances where you anticipated issues and found effective solutions. Be ready to discuss these examples during the interview to illustrate your capability in driving project consensus.
✨Emphasise Your Willingness to Learn
The client is looking for someone eager to grow. Share your experiences of continuous learning and development in your career. Discuss any recent courses or training you've undertaken that relate to regulatory affairs or medical writing to show your commitment to professional growth.
