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- Tasks: Lead regulatory documentation projects and author key documents for clinical submissions.
- Company: Global biopharmaceutical organisation with a focus on innovation.
- Benefits: Competitive salary, professional growth opportunities, and a supportive work environment.
- Why this job: Make a significant impact in drug development while advancing your career.
- Qualifications: 3+ years of regulatory writing experience and a Bachelor's degree required.
- Other info: Join a dynamic team and coach junior staff in a collaborative setting.
The predicted salary is between 36000 - 60000 £ per year.
A global biopharmaceutical organization is seeking a Senior Regulatory Writer to lead and participate in project teams focused on regulatory documentation. Candidates should have at least 3 years of regulatory writing experience and a Bachelor's degree.
This role involves:
- Authoring documents per client specifications and regulatory guidelines
- Managing project budgets
- Coaching junior staff
The ideal candidate will demonstrate strong Microsoft Word proficiency and an understanding of the drug development lifecycle. Competitive salary and opportunities for professional growth are offered.
Senior Regulatory Writer – Clinical Submissions Lead in London employer: Certara
Contact Detail:
Certara Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory Writer – Clinical Submissions Lead in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the biopharmaceutical field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Senior Regulatory Writer role.
✨Tip Number 2
Showcase your skills! Create a portfolio of your best regulatory documents and writing samples. This will give potential employers a taste of what you can bring to the table, especially your Microsoft Word prowess.
✨Tip Number 3
Prepare for interviews by brushing up on the drug development lifecycle. We recommend having specific examples ready that demonstrate your experience with regulatory documentation and project management.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Senior Regulatory Writer – Clinical Submissions Lead in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your regulatory writing experience and any relevant projects you've worked on. We want to see how your skills align with the role, so don’t be shy about showcasing your expertise in clinical submissions!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the Senior Regulatory Writer position. Share specific examples of your work that demonstrate your understanding of regulatory guidelines and the drug development lifecycle.
Show Off Your Microsoft Word Skills: Since strong Microsoft Word proficiency is key for this role, make sure to mention any advanced skills you have. Whether it's formatting complex documents or using track changes effectively, we want to know how you can make our documentation process smoother!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at Certara
✨Know Your Regulatory Stuff
Make sure you brush up on your regulatory writing knowledge. Familiarise yourself with the latest guidelines and standards in the biopharmaceutical industry. Being able to discuss specific regulations and how they apply to clinical submissions will show that you're not just experienced, but also current.
✨Showcase Your Writing Skills
Prepare samples of your previous regulatory documents to share during the interview. Highlight your ability to author documents according to client specifications and regulatory guidelines. This will give the interviewers a clear picture of your writing style and attention to detail.
✨Demonstrate Leadership Qualities
Since this role involves coaching junior staff, be ready to discuss your leadership experiences. Share examples of how you've mentored others or led project teams in the past. This will help them see you as a potential leader within their organisation.
✨Budget Management Insights
Be prepared to talk about your experience managing project budgets. Discuss any tools or strategies you’ve used to keep projects on track financially. This shows that you understand the business side of regulatory writing, which is crucial for this role.
