At a Glance
- Tasks: Support and deliver regulatory projects across UK and EU markets in a fast-paced consultancy.
- Company: DLRC Group, a leading consultancy with a strong reputation and global presence.
- Benefits: Flexible working, professional development, and a collaborative team environment.
- Other info: Opportunity for career growth and mentoring junior colleagues.
- Why this job: Join a dynamic team and make a real impact in regulatory consultancy.
- Qualifications: Experience in regulatory submissions and strong project management 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 in Letchworth employer: DLRC
At DLRC Group, we pride ourselves on being a leading consultancy that fosters a collaborative and supportive work culture. Our commitment to integrity and professional development ensures that our employees have the opportunity to grow their skills and advance their careers while working flexibly in a dynamic environment. With a diverse team of experts and a focus on delivering high-quality regulatory support, we empower our staff to make meaningful contributions to client projects and the broader regulatory landscape.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Regulatory Associate- Fixed Term Contract until 31 August 2027 in Letchworth
✨Tip Number 1
Network like a pro! Reach out to your connections in the regulatory field, attend industry events, and engage on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and its recent projects. We want to see that you’re genuinely interested in DLRC Group and understand our role in the regulatory landscape. Tailor your questions to show you’re ready to contribute to our team.
✨Tip Number 3
Showcase your expertise! Bring examples of your past regulatory submissions and project management experiences to the table. We love seeing how you’ve tackled challenges and contributed to successful outcomes in previous roles.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets the attention it deserves. Plus, we review applications on a rolling basis, so the sooner you apply, the better your chances!
We think you need these skills to ace Senior Regulatory Associate- Fixed Term Contract until 31 August 2027 in Letchworth
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter to highlight your relevant experience in regulatory submissions. We want to see how your skills align with the role, so don’t hold back on showcasing your expertise!
Showcase Your Achievements:When detailing your past roles, focus on specific achievements that demonstrate your ability to manage regulatory projects. Use numbers and examples where possible to make your application stand out to us.
Be Clear and Concise:We appreciate clarity! Keep your writing straightforward and to the point. Avoid jargon unless it’s relevant to the role, and ensure your application is easy to read and understand.
Apply Through Our Website:Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, we love seeing applications come directly from interested candidates!
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.
✨Be Ready to Discuss Submissions
Since the role involves preparing and reviewing regulatory submissions, be prepared to talk about your hands-on experience with CTAs, MAAs, and other submissions. Bring specific examples of challenges you faced and how you overcame them.
✨Emphasise Team Collaboration
This position requires a collaborative approach, so think of instances where you've worked effectively in a team. Be ready to discuss how you’ve mentored junior colleagues or contributed to knowledge sharing, as this aligns with the company’s values.
