At a Glance
- Tasks: Support and deliver regulatory projects across UK and EU markets in a fast-paced consultancy.
- Company: Join DLRC Group, a leading consultancy with a global reputation and collaborative culture.
- Benefits: Flexible working, professional development, and a supportive team environment.
- Other info: Mentorship opportunities and a chance to work with a dynamic team.
- Why this job: Make an impact in regulatory affairs while developing your strategic and project management skills.
- Qualifications: Experience in regulatory submissions and strong analytical skills required.
The predicted salary is between 40000 - 50000 £ per year.
Established in 2005, the DLRC Group has developed a deserved reputation for being a leading consultancy, with a wealth of regulatory and scientific knowledge and considerable experience in both leadership and management. The company has recently expanded to include affiliates based in Germany and the US. Our growing team comprises over 90 qualified professionals with a pharmaceutical and/or regulatory background, as well as over 30 dedicated supporting staff in areas of Business Development, Finance, Business Services and People Practices. We provide services to over 130 organisations, enabling them to achieve their strategic and operational development objectives. DLRC’s expertise and flexible working approach ensures the provision of a highly motivated team who interact effectively with clients and regulators globally, to support both single issues and long‑term commitment to projects.
We are seeking a Senior Regulatory Associate to support and deliver regulatory projects across UK and EU markets, providing high‑quality regulatory support and submissions within a fast-paced consultancy environment. This role is ideal for a regulatory professional with experience managing regulatory activities across multiple procedures who is looking to further develop their strategic, project management, and client-facing capabilities within a collaborative team.
The opportunity
You will support the delivery of regulatory projects across a range of products and procedures, preparing and reviewing regulatory submissions, contributing to regulatory strategy, and ensuring projects are delivered compliantly and on time. You will work closely with clients, internal stakeholders, and regulatory authorities while supporting junior colleagues and contributing to business development activities.
Key responsibilities
- Identify, interpret, and apply relevant UK, EU, and US regulations and guidance to support project compliance
- Prepare, review, and manage high‑quality regulatory submissions with minimal supervision
- Review documentation for accuracy, consistency, and completeness
- Contribute to regulatory recommendations and SME strategies for client projects
- Prepare submissions including CTAs, modifications, MAAs, variations, Scientific Advice requests, PIPs, and Orphan Drug applications
- Support regulatory projects, including liaison with regulatory authorities under supervision
- Monitor project risks, timelines, and action logs, proactively identifying and escalating issues
- Support project planning and stakeholder management to ensure successful project delivery
- Assist with budget management and resource planning where applicable
- Participate in business development activities including scoping calls, proposal support, and follow‑up actions
- Analyse regulatory changes and assess their impact on projects and business activities
- Mentor junior team members on routine tasks and support knowledge sharing within the team
- Ensure all activities are delivered in line with Quality Management requirements and company values
About you
- Previous hands‑on experience in preparation and management of regulatory submissions including CTA submissions in the EU and/or UK and agency interactions. Experience of submissions of other clinical development procedures (PIPs, ODD, Scientific advice) and/or post‑marketing activities is advantageous
- Good understanding of national and EU regulatory procedures
- Ability to contribute to regulatory strategy and interpret relevant legislation, guidance, and procedures
- Strong analytical skills with the ability to review complex datasets and identify inconsistencies or risks
- Understanding of scientific and regulatory environments
- Strong organisational and project management skills, including prioritisation and timeline management
- Excellent written and verbal communication skills with the ability to build strong working relationships
- Collaborative and team‑oriented approach with accountability for individual contributions
- Commercial awareness and understanding of consultancy business environments
- Ability to mentor and support the development of junior colleagues
- Degree in Life Sciences, Pharmacy, or equivalent
- Proficient in Microsoft Office applications
- Eligible to work in the UK; fluent in English
We are a consultancy built on integrity, respect, and accountability. Our people are trusted to take ownership, supported to develop, and encouraged to think commercially. We bring energy and enthusiasm to our work, collaborating closely with clients and partners to deliver practical, sustainable solutions. With flexible working and strong professional development pathways, we offer an environment where regulatory consultants can build influence, capability, and long‑term careers.
We review applications and conduct interviews on a rolling basis, so don’t delay in applying. Our Talent Acquisition team will be in touch with an update once your application has been reviewed.
Senior Regulatory Associate- Fixed Term Contract until 31 August 2027 employer: DLRC
At DLRC Group, we pride ourselves on being an exceptional employer, offering a dynamic and supportive work environment that fosters professional growth and collaboration. Our hybrid and flexible working model allows for a healthy work-life balance, while our commitment to integrity and accountability ensures that every team member is empowered to take ownership of their projects. With opportunities for mentorship and involvement in business development, we provide a platform for regulatory professionals to thrive and make a meaningful impact in the consultancy landscape.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Regulatory Associate- Fixed Term Contract until 31 August 2027
✨Tip Number 1
Network like a pro! Reach out to your connections in the regulatory field and let them know you're on the hunt for a Senior Regulatory Associate role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of UK, EU, and US regulations. Be ready to discuss how you've applied these in past roles. We want to see that you can hit the ground running and contribute to our projects right away!
✨Tip Number 3
Show off your project management skills! Be prepared to share examples of how you've successfully managed timelines and resources in previous roles. This will demonstrate your ability to keep projects compliant and on track, which is key for us.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you're genuinely interested in joining our team at DLRC Group.
We think you need these skills to ace Senior Regulatory Associate- Fixed Term Contract until 31 August 2027
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Senior Regulatory Associate role. Highlight your relevant experience in regulatory submissions and project management, as this will show us you’re a great fit for our team.
Showcase Your Skills:Don’t just list your qualifications; demonstrate how your skills align with the job description. Use specific examples from your past work that illustrate your analytical abilities and understanding of regulatory procedures.
Be Clear and Concise:When writing your application, keep it clear and to the point. We appreciate well-structured documents that are easy to read, so avoid jargon and focus on what makes you the ideal candidate for this role.
Apply Through Our Website:We encourage you to submit your application through our website. This ensures that your application is reviewed promptly by our Talent Acquisition team, and you’ll be one step closer to joining our dynamic consultancy!
How to prepare for a job interview at DLRC
✨Know Your Regulations
Make sure you brush up on the relevant UK, EU, and US regulations before your interview. Being able to discuss how these regulations apply to the role will show that you're not just familiar with the basics but can also contribute to regulatory strategy.
✨Showcase Your Project Management Skills
Prepare examples of past projects where you successfully managed timelines and stakeholder relationships. Highlighting your organisational skills and ability to handle multiple procedures will demonstrate that you’re ready for the fast-paced consultancy environment.
✨Communicate Clearly
Practice articulating your thoughts clearly and concisely. Since the role involves liaising with clients and regulatory authorities, strong verbal communication skills are essential. Consider doing mock interviews to refine your delivery.
✨Be a Team Player
Emphasise your collaborative approach during the interview. Share experiences where you mentored junior colleagues or contributed to team success. This will align with the company’s values of integrity, respect, and accountability.
