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 46000 - 52000 £ 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.
Senior Regulatory Associate - Fixed Term Contract until 31 August 2027 in Letchworth employer: DLRC Regulatory Consultancy
At DLRC Group, we pride ourselves on being a leading consultancy that fosters a collaborative and supportive work culture, where integrity and accountability are at the forefront. Our hybrid and flexible working environment allows for a healthy work-life balance, while our commitment to professional development ensures that employees have ample opportunities to grow their skills and advance their careers in the regulatory field. Join us to be part of a dynamic team that values your contributions and empowers you to make a meaningful impact in the pharmaceutical and regulatory landscape.
Contact Details:
DLRC Regulatory Consultancy Recruitment Team
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 recommend practising common interview questions and tailoring your answers to highlight your experience with regulatory submissions and project management. Show them you’re the perfect fit!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a thank-you email to express your appreciation and reiterate your interest in the role. It keeps you fresh in their minds and shows your enthusiasm for the position.
✨Tip Number 4
Apply through our website for the best chance at landing that Senior Regulatory Associate role. We make it easy for you to showcase your skills and experience directly to our hiring team. Don’t miss out on this opportunity!
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 for the Senior Regulatory Associate role. Highlight your relevant experience in regulatory submissions and project management, as this will show us you understand what we're looking for.
Showcase Your Skills:Don’t just list your qualifications; demonstrate how your skills align with our needs. Use specific examples from your past work that illustrate your ability to manage regulatory activities and contribute to strategic projects.
Be Clear and Concise:When writing your application, keep it straightforward and to the point. We appreciate clarity, so avoid jargon and ensure your key achievements stand out. This will help us quickly see why you’d be a great fit!
Apply Through Our Website:We encourage you to submit your application through our website. It’s the best way for us to receive your details directly and ensures you’re considered for the role without any hiccups!
How to prepare for a job interview at DLRC Regulatory Consultancy
✨Know Your Regulations
Make sure you brush up on the latest UK, EU, and US regulations relevant to the role. Being able to discuss specific regulations and how they apply to the projects you'll be working on will show that you're not just familiar with the basics but are ready to hit the ground running.
✨Showcase Your Project Management Skills
Prepare examples of past projects where you've successfully managed timelines, budgets, and stakeholder communications. Highlighting your organisational skills and ability to handle multiple procedures will demonstrate that you can thrive in a fast-paced consultancy environment.
✨Engage with the Team Spirit
Since this role involves collaboration, be ready to discuss how you've worked effectively within teams in the past. Share experiences where you've mentored junior colleagues or contributed to team knowledge sharing, as this aligns perfectly with the company's values.
✨Prepare for Client Interactions
Think about how you would approach client-facing situations. Be prepared to discuss how you would build strong relationships with clients and regulatory authorities, as well as how you would handle any challenges that arise during project delivery.
