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- Tasks: Lead regulatory writing projects and guide team members in creating high-quality clinical documentation.
- Company: Join Complete Regulatory, part of IPG Health, a leader in medical communications with a creative edge.
- Benefits: Enjoy flexible time off, retail discounts, private healthcare, and a supportive work environment.
- Why this job: Be part of a reputable team making a real impact in the pharmaceutical industry while developing your career.
- Qualifications: Previous experience in regulatory writing within the pharmaceutical industry or a medical writing agency is essential.
- Other info: We celebrate diversity and encourage applicants from all backgrounds to apply.
The predicted salary is between 43200 - 72000 £ per year.
Complete Regulatory is part of IPG Health Medical Communications, providing class-leading writing support and consultancy services to the pharmaceutical industry. We produce a wide range of high-quality clinical documentation, including clinical study reports, protocols, clinical summaries, clinical overviews, regulatory responses, and other supporting documents across various therapy areas.
We are looking for experienced Directors of Regulatory Writing with previous experience as a regulatory writer within the pharmaceutical industry and/or a medical writing agency. You will use your thorough knowledge of regulatory documents and development of submission documentation to lead complex submissions and guide other team members.
In this role, you will work as a trusted partner with various companies, providing high-level leadership and support on a range of project types and therapy areas. You will help maintain our excellent client relationships, consulting with clients and demonstrating your high-level strategic thinking based on extensive past experience to ensure effective medical writing for regulatory authorities.
This position will benefit anyone looking to build on their experience in regulatory writing while working within a highly specialised, supportive, and reputable team. You will be rewarded with:
- Flexible Time Off – uncapped paid time off
- Retail and gym discounts
- Great training and development
- Life assurance
- Pension
- Employee assistance programme
- Private healthcare
- Mental health wellness programme
- Cycle to work scheme
- Long Service Award
- Season Ticket Loan
- Flexible working
We celebrate diversity and encourage applicants from all backgrounds and/or disabilities. We want you to have every opportunity to shine and show us your talents, so please reach out and let us know if there are any reasonable adjustments we can make to ensure our assessment process works for you.
Director of Regulatory Writing employer: Complete Regulatory | An IPG Health Company
Contact Detail:
Complete Regulatory | An IPG Health Company Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director of Regulatory Writing
✨Tip Number 1
Familiarise yourself with the latest regulatory guidelines and trends in the pharmaceutical industry. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.
✨Tip Number 2
Network with professionals in the regulatory writing field. Attend industry conferences or webinars, and connect with current employees at Complete Regulatory on platforms like LinkedIn to gain insights into their work culture and expectations.
✨Tip Number 3
Prepare to discuss specific examples from your past experience that showcase your leadership skills and strategic thinking in regulatory writing. Be ready to explain how you've successfully managed complex submissions and maintained client relationships.
✨Tip Number 4
Research Complete Regulatory's recent projects and achievements. Being knowledgeable about their work will allow you to tailor your conversation during interviews and show genuine interest in contributing to their success.
We think you need these skills to ace Director of Regulatory Writing
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Director of Regulatory Writing. Familiarise yourself with the types of documents you'll be working on and the skills required for the role.
Tailor Your CV: Customise your CV to highlight your relevant experience in regulatory writing within the pharmaceutical industry. Emphasise your leadership skills and any successful projects you've led that align with the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for medical communications and your strategic thinking abilities. Mention specific experiences that demonstrate your expertise in regulatory writing and how you can contribute to the company's success.
Proofread Your Application: Ensure that your application is free from errors. A well-written application reflects your attention to detail, which is crucial in regulatory writing. Consider asking a colleague or friend to review it before submission.
How to prepare for a job interview at Complete Regulatory | An IPG Health Company
✨Showcase Your Regulatory Knowledge
Make sure to highlight your understanding of regulatory documents and submission processes during the interview. Be prepared to discuss specific examples from your past experience that demonstrate your expertise in this area.
✨Demonstrate Leadership Skills
As a Director of Regulatory Writing, you'll need to lead teams and guide others. Share instances where you've successfully led projects or mentored colleagues, showcasing your ability to inspire and support your team.
✨Emphasise Client Relationship Management
Since maintaining excellent client relationships is crucial, be ready to talk about how you've built and nurtured client partnerships in previous roles. Discuss your approach to strategic thinking and problem-solving in client interactions.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your decision-making and critical thinking skills. Practice articulating your thought process and how you would handle complex regulatory writing challenges that may arise in the role.
