Senior Regulatory Writer & Project Lead in London
Senior Regulatory Writer & Project Lead

Senior Regulatory Writer & Project Lead in London

London Full-Time 42000 - 84000 £ / year (est.) No home office possible
C

At a Glance

  • Tasks: Create high-quality regulatory documents and lead project teams in drug development.
  • Company: Leading strategic drug development firm in the UK with a collaborative culture.
  • Benefits: Opportunity to make a positive impact on drug development and work with clients.
  • Why this job: Join a dynamic team and contribute to meaningful projects in healthcare.
  • Qualifications: 5+ years of regulatory writing experience and a relevant degree.
  • Other info: Collaborative environment with opportunities for professional growth.

The predicted salary is between 42000 - 84000 £ per year.

A leading strategic drug development firm in the United Kingdom seeks an Associate Principal Regulatory Writer. The role involves authoring high-quality documents for regulatory submissions, leading project teams, and collaborating closely with clients.

The ideal candidate will have over 5 years of regulatory writing experience, a Bachelor's degree or higher, and strong skills in document preparation.

This position offers a chance to impact drug development positively, working in a collaborative environment.

Senior Regulatory Writer & Project Lead in London employer: Certara

As a leading strategic drug development firm in the United Kingdom, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to make a meaningful impact in the field of drug development. We offer competitive benefits, continuous professional growth opportunities, and a supportive environment where your expertise as a Senior Regulatory Writer & Project Lead will be valued and recognised. Join us to be part of a team that is dedicated to advancing healthcare and improving patient outcomes.
C

Contact Detail:

Certara Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Regulatory Writer & Project Lead in London

✨Tip Number 1

Network like a pro! Reach out to professionals in the regulatory writing field on LinkedIn or at industry events. Building connections can lead to job opportunities that aren’t even advertised yet.

✨Tip Number 2

Showcase your expertise! Prepare a portfolio of your best regulatory documents and be ready to discuss them in interviews. This will demonstrate your skills and give you an edge over other candidates.

✨Tip Number 3

Practice makes perfect! Conduct mock interviews with friends or mentors, focusing on common questions for regulatory writers. This will help you articulate your experience and confidence during the real deal.

✨Tip Number 4

Don’t forget to apply through our website! We regularly update our job listings, and applying directly can sometimes give you a better chance of landing that interview. Let’s get you that dream job!

We think you need these skills to ace Senior Regulatory Writer & Project Lead in London

Regulatory Writing
Document Preparation
Project Leadership
Collaboration Skills
Client Management
Attention to Detail
Communication Skills
Drug Development Knowledge
Analytical Skills
Time Management
Team Coordination
Quality Assurance

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your regulatory writing experience and any relevant projects you've led. We want to see how your background aligns with the role, so don’t be shy about showcasing your skills!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about regulatory writing and how you can contribute to our team. Keep it concise but impactful – we love a good story!

Showcase Your Teamwork Skills: Since collaboration is key in this role, mention any experiences where you’ve successfully worked with clients or project teams. We’re looking for someone who thrives in a team environment, so let us know how you fit that bill!

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’s super easy – just a few clicks and you’re done!

How to prepare for a job interview at Certara

✨Know Your Regulatory Stuff

Make sure you brush up on the latest regulations and guidelines relevant to drug development. Being able to discuss specific examples of your past regulatory writing experience will show that you’re not just familiar with the rules, but that you can apply them effectively.

✨Showcase Your Leadership Skills

As a project lead, you'll need to demonstrate your ability to lead teams. Prepare examples of how you've successfully managed projects in the past, highlighting your collaboration with clients and team members. This will help convey your leadership style and effectiveness.

✨Prepare High-Quality Documents

Since the role involves authoring high-quality documents, bring samples of your previous work to the interview. Be ready to discuss your writing process, how you ensure accuracy, and how you handle feedback. This will give the interviewers confidence in your document preparation skills.

✨Ask Insightful Questions

Don’t forget to prepare some thoughtful questions about the company’s approach to drug development and their expectations for the role. This shows your genuine interest in the position and helps you assess if it’s the right fit for you.

Senior Regulatory Writer & Project Lead in London
Certara
Location: London

Land your dream job quicker with Premium

You’re marked as a top applicant with our partner companies
Individual CV and cover letter feedback including tailoring to specific job roles
Be among the first applications for new jobs with our AI application
1:1 support and career advice from our career coaches
Go Premium

Money-back if you don't land a job in 6-months

C
Similar positions in other companies
UK’s top job board for Gen Z
discover-jobs-cta
Discover now
>